Bonvalotidine A acetone solvate from Delphinium bonvalotii Franch

Li, S.-H.; Chen, F.-Z.

doi:10.1107/S1600536810047562

organic compounds

CRYSTALLOGRAPHIC
COMMUNICATIONS

ISSN: 2056-9890

Volume 66| Part 12| December 2010| Page o3319

https://doi.org/10.1107/S1600536810047562

Open

access

Bonvalotidine A acetone solvate from Delphinium bonvalotii Franch

Shu-Hua Li ^a and Feng-Zheng Chen ^a ^*

^aDepartment of Chemistry and Life Sciences, Leshan Teachers College, Leshan 614004, People's Republic of China
^*Correspondence e-mail: fzchen7200@163.com

(Received 28 October 2010; accepted 16 November 2010; online 27 November 2010)

The title compound (systematic name: 5,6β-dihydroxy-1α,14α,16β-trimethoxy-4-methyl-7β,8-methylenedioxy-20-ethylaconitan-6-yl acetate acetone monosolvate), C₂₇H₄₁NO₈·C₃H₆O, was isolated from Delphinium bonvalotii Franch, and is a typical C₁₉-diterpenoid alkaloid. The molecule has a lycoctonine carbon skeleton with four six-membered rings and three five-membered rings. Three six-membered rings adopt the chair conformations while the fourth adopts a boat conformation, while the five-membered rings have the envelope conformations. The solvent molecule links with the organic molecule via a classical O—H⋯O hydrogen bond. Weak C—H⋯O hydrogen bonding is present in the structure. An intramolecular O—H⋯O hydrogen bond also occurs.

Related literature

For the chemical structure of the title compound established from NMR and MS data, see: He et al. (2006 ). For the crystal structures of related C₁₉-diterpenoid alkaloids, see: Wang et al. (2009 ).

Experimental

Crystal data

C₂₇H₄₁NO₈·C₃H₆O
M_r = 565.69
Orthorhombic, P 2₁ 2₁ 2₁
a = 8.4260 (8) Å
b = 9.5546 (7) Å
c = 35.237 (3) Å
V = 2836.8 (4) Å³
Z = 4
Mo Kα radiation
μ = 0.10 mm⁻¹
T = 120 K
0.42 × 0.36 × 0.21 mm

Data collection

Oxford Diffraction Xcalibur Eos diffractometer
9839 measured reflections
2930 independent reflections
2690 reflections with I > 2σ(I)
R_int = 0.022

Refinement

R[F² > 2σ(F²)] = 0.044
wR(F²) = 0.104
S = 1.08
2930 reflections
373 parameters
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.69 e Å⁻³
Δρ_min = −0.27 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O2—H2⋯O3	0.99 (5)	2.00 (5)	2.605 (3)	118 (4)
O2—H2⋯O9	0.99 (5)	2.13 (5)	2.936 (4)	138 (4)
C24—H24A⋯O9	0.98	2.53	3.427 (5)	153
C25—H25A⋯O2ⁱ	0.99	2.36	3.344 (4)	170
Symmetry code: (i) x-1, y, z.

Data collection: CrysAlis CCD (Oxford Diffraction, 2008 $[Oxford Diffraction (2008). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Yarnton, England.]$ ); cell refinement: CrysAlis RED (Oxford Diffraction, 2008 $[Oxford Diffraction (2008). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Yarnton, England.]$ ); data reduction: CrysAlis RED; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: OLEX2 (Dolomanov et al. 2009 ); software used to prepare material for publication: SHELXL97.

Supporting information

Crystal structure: contains datablocks I, global. DOI: https://doi.org/10.1107/S1600536810047562/xu5072sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810047562/xu5072Isup2.hkl

checkCIF report

Comment top

The title compound, bonvalotidine A, was previously isolated from Delphinium bonvalotii Franch (He et al. 2006), and its structure was established from the NMR and MS data. In our recent investigation, it was isolation from the root of Delphinium bonvalotii Franch collected in the E'mei Mountain, Sichuan Province of P. R. China in September, 2009. A nd its crystal structure was determined. The naming conforming referred to the literature (Wang et al. 2009). The molecular structure of the title compound is shown in Fig. 1. Six-membered rings A (C1/C2/C3/C4/C5/C11) and B (C7/C8/C9/C10/C11/C17) adopt chair conformations; six-membered ring D (C8/C9/C14/C13/C16/C15) adopt a boat conformation; six-membered N-containing heterocyclic ring E (C4/C5/C11/C17/N1/C19) displays the same chair conformation; five-membered rings C (C9/C10/C12/C13/C14) and F (C5/C6/C7/C17/C11) adopt an envelope conformation. While the five-membered O-containing heterocyclic G (O5/C7/C8/O6/C25) displays an envelope conformation.

The crystal structure contains intermolecular O—H···O hydrogen bond between the hydroxyl group and carbonyl O atom. The lattice acetone molecule links with the organic molecule via O—H···O hydrogen is present in the crystal structure (Table 1).

Related literature top

For the chemical structure of the title compound established from NMR and MS data, see: He et al. (2006). For the crystal structures of related C₁₉-diterpenoid alkaloids, see: Wang et al. (2009).

Experimental top

The title compound was isolated from the root of Delphinium bonvalotii Franch. Single crystals suitable for X-ray structure analysis were obtained by slow evaporation from an acetone solution at room temperature.

Structure description top

For the chemical structure of the title compound established from NMR and MS data, see: He et al. (2006). For the crystal structures of related C₁₉-diterpenoid alkaloids, see: Wang et al. (2009).

Computing details top

Data collection: CrysAlis CCD (Oxford Diffraction, 2008); cell refinement: CrysAlis RED (Oxford Diffraction, 2008); data reduction: CrysAlis RED (Oxford Diffraction, 2008); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: OLEX2 (Dolomanov et al. 2009); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top

Fig. 1. The molecular structure of thetitle compound with 30% probabiliy displacement ellipsoids for no-H atoms. Hatoms have been omitted clarity. Dashed line indicates hydrogen bonding.

5,6β-dihydroxy-1α,14α,16β-trimethoxy-4-methyl-7β,8-methylenedioxy- 20-ethylaconitan-6-yl acetate acetone monosolvate top

Crystal data top

C₂₇H₄₁NO₈·C₃H₆O	F(000) = 1224
M_r = 565.69	D_x = 1.324 Mg m⁻³
Orthorhombic, P2₁2₁2₁	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ac 2ab	Cell parameters from 6568 reflections
a = 8.4260 (8) Å	θ = 3.1–25.0°
b = 9.5546 (7) Å	µ = 0.10 mm⁻¹
c = 35.237 (3) Å	T = 120 K
V = 2836.8 (4) Å³	Block, colorless
Z = 4	0.42 × 0.36 × 0.21 mm

Data collection top

Oxford Diffraction Xcalibur Eos diffractometer	2690 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.022
Graphite monochromator	θ_max = 25.2°, θ_min = 3.2°
ω scan	h = −10→9
9839 measured reflections	k = −11→11
2930 independent reflections	l = −22→42

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.044	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.104	H atoms treated by a mixture of independent and constrained refinement
S = 1.08	w = 1/[σ²(F_o²) + (0.0438P)² + 2.2374P] where P = (F_o² + 2F_c²)/3
2930 reflections	(Δ/σ)_max = 0.002
373 parameters	Δρ_max = 0.69 e Å⁻³
0 restraints	Δρ_min = −0.27 e Å⁻³

Crystal data top

C₂₇H₄₁NO₈·C₃H₆O	V = 2836.8 (4) Å³
M_r = 565.69	Z = 4
Orthorhombic, P2₁2₁2₁	Mo Kα radiation
a = 8.4260 (8) Å	µ = 0.10 mm⁻¹
b = 9.5546 (7) Å	T = 120 K
c = 35.237 (3) Å	0.42 × 0.36 × 0.21 mm

Data collection top

Oxford Diffraction Xcalibur Eos diffractometer	2690 reflections with I > 2σ(I)
9839 measured reflections	R_int = 0.022
2930 independent reflections

Refinement top

R[F² > 2σ(F²)] = 0.044	0 restraints
wR(F²) = 0.104	H atoms treated by a mixture of independent and constrained refinement
S = 1.08	Δρ_max = 0.69 e Å⁻³
2930 reflections	Δρ_min = −0.27 e Å⁻³
373 parameters

Special details top

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.

Refinement. Refinement of F² against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F², conventional R-factors R are based on F, with F set to zero for negative F². The threshold expression of F² > σ(F²) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F² are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
O1	0.6059 (3)	0.7225 (2)	0.47254 (6)	0.0246 (5)
O2	0.7919 (3)	0.6104 (3)	0.35691 (7)	0.0269 (6)
O3	0.5491 (3)	0.5711 (2)	0.31240 (6)	0.0184 (5)
O4	0.4301 (4)	0.3889 (3)	0.28401 (7)	0.0398 (7)
O5	0.2412 (3)	0.4687 (2)	0.36445 (6)	0.0189 (5)
O6	0.2372 (3)	0.6543 (2)	0.32229 (6)	0.0186 (5)
O7	0.2550 (3)	0.9818 (2)	0.32957 (6)	0.0223 (5)
O8	0.0416 (3)	0.9541 (3)	0.40687 (7)	0.0329 (6)
O9	0.8945 (3)	0.6682 (3)	0.27882 (8)	0.0436 (7)
N1	0.4624 (3)	0.4363 (3)	0.43288 (7)	0.0173 (6)
C1	0.6960 (4)	0.6670 (3)	0.44119 (9)	0.0231 (7)
H1	0.7796	0.7371	0.4345	0.028*
C2	0.7798 (4)	0.5360 (4)	0.45604 (10)	0.0271 (8)
H2A	0.8683	0.5645	0.4728	0.033*
H2B	0.7041	0.4806	0.4714	0.033*
C3	0.8446 (4)	0.4447 (4)	0.42437 (10)	0.0271 (8)
H3A	0.8870	0.3568	0.4353	0.033*
H3B	0.9332	0.4940	0.4116	0.033*
C4	0.7166 (4)	0.4097 (3)	0.39515 (9)	0.0214 (7)
C5	0.6632 (4)	0.5480 (3)	0.37573 (9)	0.0182 (7)
C6	0.5217 (4)	0.5115 (3)	0.34940 (8)	0.0161 (6)
H6	0.5173	0.4074	0.3466	0.019*
C7	0.3717 (4)	0.5591 (3)	0.37131 (9)	0.0151 (6)
C8	0.3050 (4)	0.7005 (3)	0.35823 (9)	0.0180 (7)
C9	0.4386 (4)	0.8063 (3)	0.35323 (8)	0.0161 (6)
H9	0.4963	0.7901	0.3288	0.019*
C10	0.5551 (4)	0.7971 (3)	0.38791 (9)	0.0191 (7)
H10	0.6599	0.8331	0.3789	0.023*
C11	0.5873 (4)	0.6482 (3)	0.40582 (9)	0.0169 (7)
C12	0.4868 (5)	0.9106 (3)	0.41606 (9)	0.0287 (8)
H12A	0.4622	0.8675	0.4409	0.034*
H12B	0.5654	0.9862	0.4200	0.034*
C13	0.3358 (4)	0.9694 (3)	0.39794 (9)	0.0255 (8)
H13	0.3195	1.0693	0.4054	0.031*
C14	0.3782 (4)	0.9577 (3)	0.35576 (9)	0.0204 (7)
H14	0.4680	1.0229	0.3501	0.024*
C15	0.1656 (4)	0.7551 (3)	0.38249 (10)	0.0232 (7)
H15B	0.0782	0.7794	0.3649	0.028*
H15A	0.1278	0.6763	0.3983	0.028*
C16	0.1906 (4)	0.8800 (3)	0.40873 (9)	0.0257 (8)
H16	0.2056	0.8445	0.4352	0.031*
C17	0.4316 (4)	0.5675 (3)	0.41273 (8)	0.0158 (6)
H17	0.3575	0.6267	0.4280	0.019*
C18	0.7886 (4)	0.3079 (4)	0.36619 (10)	0.0284 (8)
H18B	0.8907	0.3444	0.3573	0.043*
H18C	0.7162	0.2978	0.3446	0.043*
H18A	0.8047	0.2164	0.3782	0.043*
C19	0.5701 (4)	0.3402 (3)	0.41337 (9)	0.0202 (7)
H19B	0.5099	0.2908	0.3933	0.024*
H19A	0.6069	0.2690	0.4318	0.024*
C20	0.3177 (4)	0.3659 (3)	0.44604 (9)	0.0234 (7)
H20B	0.2703	0.3131	0.4247	0.028*
H20A	0.2397	0.4371	0.4543	0.028*
C21	0.3508 (5)	0.2660 (4)	0.47871 (10)	0.0301 (8)
H21C	0.4115	0.1856	0.4694	0.045*
H21B	0.2502	0.2336	0.4895	0.045*
H21A	0.4122	0.3146	0.4983	0.045*
C22	0.6932 (5)	0.8197 (4)	0.49485 (10)	0.0325 (9)
H22B	0.7969	0.7796	0.5012	0.049*
H22A	0.6346	0.8399	0.5182	0.049*
H22C	0.7084	0.9064	0.4805	0.049*
C23	0.4946 (4)	0.5004 (3)	0.28192 (9)	0.0241 (7)
C24	0.5246 (5)	0.5798 (4)	0.24627 (9)	0.0305 (9)
H24C	0.5160	0.5165	0.2245	0.046*
H24A	0.6313	0.6204	0.2471	0.046*
H24B	0.4460	0.6549	0.2438	0.046*
C25	0.1621 (4)	0.5249 (3)	0.33175 (9)	0.0215 (7)
H25B	0.1700	0.4587	0.3102	0.026*
H25A	0.0484	0.5406	0.3374	0.026*
C26	0.2066 (5)	1.1253 (3)	0.32951 (10)	0.0296 (8)
H26A	0.1479	1.1457	0.3529	0.044*
H26C	0.1383	1.1429	0.3075	0.044*
H26B	0.3006	1.1856	0.3281	0.044*
C27	0.0114 (5)	1.0354 (4)	0.43882 (11)	0.0390 (9)
H27A	0.0191	0.9770	0.4616	0.059*
H27C	−0.0955	1.0752	0.4370	0.059*
H27B	0.0895	1.1112	0.4403	0.059*
C28	0.9445 (5)	0.7871 (4)	0.27569 (11)	0.0359 (9)
C29	1.0840 (5)	0.8220 (5)	0.25177 (11)	0.0398 (10)
H29C	1.1123	0.7409	0.2362	0.060*
H29A	1.1739	0.8469	0.2681	0.060*
H29B	1.0580	0.9013	0.2353	0.060*
C30	0.8676 (6)	0.9039 (5)	0.29680 (14)	0.0504 (12)
H30B	0.7676	0.8711	0.3079	0.076*
H30C	0.8460	0.9814	0.2793	0.076*
H30A	0.9384	0.9361	0.3171	0.076*
H2	0.769 (5)	0.618 (5)	0.3296 (13)	0.059 (14)*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
O1	0.0318 (13)	0.0243 (12)	0.0178 (11)	−0.0064 (11)	−0.0067 (10)	0.0012 (10)
O2	0.0167 (12)	0.0326 (13)	0.0315 (14)	−0.0044 (10)	0.0015 (11)	0.0099 (11)
O3	0.0217 (11)	0.0168 (11)	0.0165 (10)	−0.0010 (9)	0.0041 (9)	−0.0009 (9)
O4	0.0657 (19)	0.0266 (13)	0.0271 (13)	−0.0164 (14)	0.0058 (14)	−0.0070 (11)
O5	0.0163 (10)	0.0202 (11)	0.0203 (11)	−0.0043 (10)	−0.0014 (9)	0.0020 (9)
O6	0.0179 (11)	0.0204 (11)	0.0174 (11)	−0.0032 (10)	−0.0009 (9)	0.0010 (9)
O7	0.0299 (12)	0.0156 (11)	0.0214 (11)	0.0038 (10)	−0.0032 (11)	0.0038 (9)
O8	0.0400 (14)	0.0306 (13)	0.0281 (13)	0.0117 (13)	0.0030 (12)	−0.0015 (12)
O9	0.0386 (16)	0.0432 (16)	0.0491 (17)	−0.0146 (14)	−0.0111 (14)	0.0109 (14)
N1	0.0213 (13)	0.0133 (12)	0.0175 (12)	−0.0007 (11)	0.0019 (11)	0.0027 (11)
C1	0.0236 (17)	0.0188 (16)	0.0270 (17)	−0.0058 (14)	−0.0051 (15)	0.0059 (14)
C2	0.0289 (18)	0.0255 (17)	0.0268 (17)	−0.0038 (16)	−0.0118 (16)	0.0082 (15)
C3	0.0211 (16)	0.0280 (17)	0.0323 (19)	0.0018 (16)	−0.0058 (16)	0.0121 (16)
C4	0.0194 (16)	0.0182 (15)	0.0265 (17)	0.0022 (14)	0.0038 (14)	0.0054 (14)
C5	0.0142 (15)	0.0175 (15)	0.0230 (16)	−0.0006 (13)	0.0002 (14)	0.0056 (14)
C6	0.0198 (15)	0.0131 (14)	0.0153 (15)	−0.0009 (13)	0.0045 (13)	0.0031 (12)
C7	0.0155 (15)	0.0146 (14)	0.0152 (15)	−0.0039 (13)	0.0002 (13)	−0.0016 (13)
C8	0.0195 (16)	0.0187 (15)	0.0157 (15)	0.0025 (13)	−0.0004 (13)	0.0001 (13)
C9	0.0215 (15)	0.0149 (14)	0.0118 (14)	0.0003 (13)	−0.0011 (13)	0.0013 (12)
C10	0.0260 (17)	0.0144 (15)	0.0171 (15)	−0.0048 (14)	−0.0060 (14)	0.0024 (13)
C11	0.0192 (16)	0.0148 (15)	0.0166 (15)	−0.0022 (13)	−0.0038 (13)	0.0036 (12)
C12	0.048 (2)	0.0183 (16)	0.0202 (16)	0.0011 (17)	−0.0103 (17)	−0.0036 (14)
C13	0.043 (2)	0.0161 (15)	0.0170 (16)	0.0085 (16)	−0.0071 (15)	−0.0017 (13)
C14	0.0310 (18)	0.0135 (14)	0.0167 (15)	0.0001 (14)	−0.0027 (15)	0.0020 (13)
C15	0.0216 (16)	0.0235 (16)	0.0246 (17)	0.0042 (15)	0.0049 (14)	0.0022 (14)
C16	0.037 (2)	0.0241 (17)	0.0161 (16)	0.0129 (16)	0.0013 (15)	0.0044 (14)
C17	0.0185 (15)	0.0127 (14)	0.0162 (15)	−0.0012 (13)	0.0005 (13)	−0.0014 (13)
C18	0.0256 (18)	0.0260 (17)	0.0334 (19)	0.0099 (15)	0.0078 (16)	0.0069 (15)
C19	0.0223 (16)	0.0166 (15)	0.0218 (16)	0.0007 (14)	0.0025 (14)	0.0053 (13)
C20	0.0256 (17)	0.0221 (16)	0.0227 (17)	−0.0020 (15)	0.0062 (15)	0.0038 (14)
C21	0.037 (2)	0.0283 (18)	0.0254 (19)	−0.0100 (17)	0.0003 (16)	0.0055 (15)
C22	0.041 (2)	0.0332 (19)	0.0238 (18)	−0.0082 (18)	−0.0118 (17)	0.0003 (16)
C23	0.0291 (17)	0.0205 (16)	0.0226 (17)	0.0002 (15)	0.0054 (15)	−0.0046 (14)
C24	0.036 (2)	0.036 (2)	0.0194 (16)	−0.0043 (18)	0.0030 (16)	0.0003 (15)
C25	0.0187 (15)	0.0217 (16)	0.0241 (17)	−0.0033 (14)	−0.0024 (14)	0.0023 (14)
C26	0.043 (2)	0.0215 (17)	0.0241 (18)	0.0090 (16)	−0.0003 (17)	0.0026 (14)
C27	0.036 (2)	0.044 (2)	0.037 (2)	0.007 (2)	0.0103 (18)	−0.0029 (18)
C28	0.0307 (19)	0.041 (2)	0.036 (2)	−0.0108 (18)	−0.0177 (18)	0.0152 (19)
C29	0.043 (2)	0.045 (2)	0.032 (2)	−0.008 (2)	−0.0068 (19)	0.0083 (19)
C30	0.041 (2)	0.048 (3)	0.062 (3)	−0.003 (2)	0.001 (2)	0.017 (2)

Geometric parameters (Å, º) top

O1—C22	1.421 (4)	C12—C13	1.531 (5)
O1—C1	1.442 (4)	C12—H12A	0.9900
O2—C5	1.404 (4)	C12—H12B	0.9900
O2—H2	0.99 (5)	C13—C14	1.533 (4)
O3—C23	1.349 (4)	C13—C16	1.540 (5)
O3—C6	1.441 (3)	C13—H13	1.0000
O4—C23	1.198 (4)	C14—H14	1.0000
O5—C7	1.419 (4)	C15—C16	1.524 (5)
O5—C25	1.436 (4)	C15—H15B	0.9900
O6—C25	1.429 (4)	C15—H15A	0.9900
O6—C8	1.457 (4)	C16—H16	1.0000
O7—C14	1.408 (4)	C17—H17	1.0000
O7—C26	1.431 (4)	C18—H18B	0.9800
O8—C27	1.391 (4)	C18—H18C	0.9800
O8—C16	1.443 (4)	C18—H18A	0.9800
O9—C28	1.217 (5)	C19—H19B	0.9900
N1—C19	1.462 (4)	C19—H19A	0.9900
N1—C17	1.464 (4)	C20—C21	1.521 (4)
N1—C20	1.468 (4)	C20—H20B	0.9900
C1—C2	1.530 (5)	C20—H20A	0.9900
C1—C11	1.557 (4)	C21—H21C	0.9800
C1—H1	1.0000	C21—H21B	0.9800
C2—C3	1.518 (5)	C21—H21A	0.9800
C2—H2A	0.9900	C22—H22B	0.9800
C2—H2B	0.9900	C22—H22A	0.9800
C3—C4	1.528 (5)	C22—H22C	0.9800
C3—H3A	0.9900	C23—C24	1.489 (5)
C3—H3B	0.9900	C24—H24C	0.9800
C4—C18	1.535 (5)	C24—H24A	0.9800
C4—C19	1.542 (4)	C24—H24B	0.9800
C4—C5	1.555 (4)	C25—H25B	0.9900
C5—C6	1.550 (4)	C25—H25A	0.9900
C5—C11	1.566 (4)	C26—H26A	0.9800
C6—C7	1.549 (4)	C26—H26C	0.9800
C6—H6	1.0000	C26—H26B	0.9800
C7—C8	1.534 (4)	C27—H27A	0.9800
C7—C17	1.547 (4)	C27—H27C	0.9800
C8—C9	1.523 (4)	C27—H27B	0.9800
C8—C15	1.544 (4)	C28—C29	1.484 (6)
C9—C14	1.536 (4)	C28—C30	1.490 (6)
C9—C10	1.570 (4)	C29—H29C	0.9800
C9—H9	1.0000	C29—H29A	0.9800
C10—C12	1.578 (4)	C29—H29B	0.9800
C10—C11	1.579 (4)	C30—H30B	0.9800
C10—H10	1.0000	C30—H30C	0.9800
C11—C17	1.541 (4)	C30—H30A	0.9800

C22—O1—C1	113.1 (3)	C13—C14—H14	109.0
C5—O2—H2	110 (3)	C9—C14—H14	109.0
C23—O3—C6	117.9 (2)	C16—C15—C8	119.7 (3)
C7—O5—C25	105.6 (2)	C16—C15—H15B	107.4
C25—O6—C8	103.5 (2)	C8—C15—H15B	107.4
C14—O7—C26	111.6 (3)	C16—C15—H15A	107.4
C27—O8—C16	113.3 (3)	C8—C15—H15A	107.4
C19—N1—C17	114.8 (2)	H15B—C15—H15A	106.9
C19—N1—C20	112.1 (2)	O8—C16—C15	103.7 (3)
C17—N1—C20	113.5 (2)	O8—C16—C13	114.1 (3)
O1—C1—C2	106.4 (3)	C15—C16—C13	113.2 (3)
O1—C1—C11	110.2 (3)	O8—C16—H16	108.5
C2—C1—C11	116.8 (3)	C15—C16—H16	108.5
O1—C1—H1	107.7	C13—C16—H16	108.5
C2—C1—H1	107.7	N1—C17—C11	110.7 (2)
C11—C1—H1	107.7	N1—C17—C7	118.1 (2)
C3—C2—C1	112.6 (3)	C11—C17—C7	98.9 (2)
C3—C2—H2A	109.1	N1—C17—H17	109.5
C1—C2—H2A	109.1	C11—C17—H17	109.5
C3—C2—H2B	109.1	C7—C17—H17	109.5
C1—C2—H2B	109.1	C4—C18—H18B	109.5
H2A—C2—H2B	107.8	C4—C18—H18C	109.5
C2—C3—C4	111.5 (3)	H18B—C18—H18C	109.5
C2—C3—H3A	109.3	C4—C18—H18A	109.5
C4—C3—H3A	109.3	H18B—C18—H18A	109.5
C2—C3—H3B	109.3	H18C—C18—H18A	109.5
C4—C3—H3B	109.3	N1—C19—C4	115.0 (3)
H3A—C3—H3B	108.0	N1—C19—H19B	108.5
C3—C4—C18	107.9 (3)	C4—C19—H19B	108.5
C3—C4—C19	112.3 (3)	N1—C19—H19A	108.5
C18—C4—C19	108.7 (3)	C4—C19—H19A	108.5
C3—C4—C5	108.4 (3)	H19B—C19—H19A	107.5
C18—C4—C5	111.1 (3)	N1—C20—C21	112.0 (3)
C19—C4—C5	108.5 (2)	N1—C20—H20B	109.2
O2—C5—C6	114.0 (3)	C21—C20—H20B	109.2
O2—C5—C4	110.2 (2)	N1—C20—H20A	109.2
C6—C5—C4	107.2 (2)	C21—C20—H20A	109.2
O2—C5—C11	112.0 (3)	H20B—C20—H20A	107.9
C6—C5—C11	103.2 (2)	C20—C21—H21C	109.5
C4—C5—C11	109.9 (3)	C20—C21—H21B	109.5
O3—C6—C7	117.8 (2)	H21C—C21—H21B	109.5
O3—C6—C5	109.2 (2)	C20—C21—H21A	109.5
C7—C6—C5	105.3 (2)	H21C—C21—H21A	109.5
O3—C6—H6	108.1	H21B—C21—H21A	109.5
C7—C6—H6	108.1	O1—C22—H22B	109.5
C5—C6—H6	108.1	O1—C22—H22A	109.5
O5—C7—C8	101.6 (2)	H22B—C22—H22A	109.5
O5—C7—C17	116.4 (2)	O1—C22—H22C	109.5
C8—C7—C17	110.9 (2)	H22B—C22—H22C	109.5
O5—C7—C6	111.6 (2)	H22A—C22—H22C	109.5
C8—C7—C6	114.1 (2)	O4—C23—O3	123.4 (3)
C17—C7—C6	102.7 (2)	O4—C23—C24	125.6 (3)
O6—C8—C9	112.9 (2)	O3—C23—C24	111.0 (3)
O6—C8—C7	98.0 (2)	C23—C24—H24C	109.5
C9—C8—C7	110.4 (2)	C23—C24—H24A	109.5
O6—C8—C15	106.6 (2)	H24C—C24—H24A	109.5
C9—C8—C15	113.7 (3)	C23—C24—H24B	109.5
C7—C8—C15	114.2 (3)	H24C—C24—H24B	109.5
C8—C9—C14	112.0 (3)	H24A—C24—H24B	109.5
C8—C9—C10	109.6 (2)	O6—C25—O5	107.8 (2)
C14—C9—C10	102.4 (2)	O6—C25—H25B	110.2
C8—C9—H9	110.9	O5—C25—H25B	110.2
C14—C9—H9	110.9	O6—C25—H25A	110.2
C10—C9—H9	110.9	O5—C25—H25A	110.2
C9—C10—C12	102.9 (2)	H25B—C25—H25A	108.5
C9—C10—C11	118.0 (2)	O7—C26—H26A	109.5
C12—C10—C11	115.5 (2)	O7—C26—H26C	109.5
C9—C10—H10	106.6	H26A—C26—H26C	109.5
C12—C10—H10	106.6	O7—C26—H26B	109.5
C11—C10—H10	106.6	H26A—C26—H26B	109.5
C17—C11—C1	115.6 (2)	H26C—C26—H26B	109.5
C17—C11—C5	98.5 (2)	O8—C27—H27A	109.5
C1—C11—C5	111.9 (3)	O8—C27—H27C	109.5
C17—C11—C10	111.6 (2)	H27A—C27—H27C	109.5
C1—C11—C10	108.5 (2)	O8—C27—H27B	109.5
C5—C11—C10	110.5 (2)	H27A—C27—H27B	109.5
C13—C12—C10	107.1 (3)	H27C—C27—H27B	109.5
C13—C12—H12A	110.3	O9—C28—C29	122.4 (4)
C10—C12—H12A	110.3	O9—C28—C30	120.2 (4)
C13—C12—H12B	110.3	C29—C28—C30	117.4 (3)
C10—C12—H12B	110.3	C28—C29—H29C	109.5
H12A—C12—H12B	108.6	C28—C29—H29A	109.5
C12—C13—C14	100.6 (3)	H29C—C29—H29A	109.5
C12—C13—C16	110.7 (3)	C28—C29—H29B	109.5
C14—C13—C16	112.6 (3)	H29C—C29—H29B	109.5
C12—C13—H13	110.8	H29A—C29—H29B	109.5
C14—C13—H13	110.8	C28—C30—H30B	109.5
C16—C13—H13	110.8	C28—C30—H30C	109.5
O7—C14—C13	116.8 (3)	H30B—C30—H30C	109.5
O7—C14—C9	111.1 (2)	C28—C30—H30A	109.5
C13—C14—C9	101.7 (2)	H30B—C30—H30A	109.5
O7—C14—H14	109.0	H30C—C30—H30A	109.5

C22—O1—C1—C2	89.7 (3)	O2—C5—C11—C1	−72.0 (3)
C22—O1—C1—C11	−142.7 (3)	C6—C5—C11—C1	164.8 (2)
O1—C1—C2—C3	165.1 (3)	C4—C5—C11—C1	50.8 (3)
C11—C1—C2—C3	41.5 (4)	O2—C5—C11—C10	49.0 (3)
C1—C2—C3—C4	−52.8 (4)	C6—C5—C11—C10	−74.2 (3)
C2—C3—C4—C18	−175.4 (3)	C4—C5—C11—C10	171.8 (2)
C2—C3—C4—C19	−55.6 (4)	C9—C10—C11—C17	−47.6 (4)
C2—C3—C4—C5	64.2 (3)	C12—C10—C11—C17	74.5 (3)
C3—C4—C5—O2	61.2 (3)	C9—C10—C11—C1	−176.1 (3)
C18—C4—C5—O2	−57.2 (4)	C12—C10—C11—C1	−53.9 (4)
C19—C4—C5—O2	−176.6 (3)	C9—C10—C11—C5	60.9 (4)
C3—C4—C5—C6	−174.2 (2)	C12—C10—C11—C5	−176.9 (3)
C18—C4—C5—C6	67.4 (3)	C9—C10—C12—C13	3.4 (3)
C19—C4—C5—C6	−52.1 (3)	C11—C10—C12—C13	−126.5 (3)
C3—C4—C5—C11	−62.7 (3)	C10—C12—C13—C14	−31.9 (3)
C18—C4—C5—C11	178.8 (3)	C10—C12—C13—C16	87.4 (3)
C19—C4—C5—C11	59.4 (3)	C26—O7—C14—C13	68.7 (4)
C23—O3—C6—C7	−93.5 (3)	C26—O7—C14—C9	−175.3 (3)
C23—O3—C6—C5	146.6 (3)	C12—C13—C14—O7	169.9 (3)
O2—C5—C6—O3	−8.6 (3)	C16—C13—C14—O7	52.0 (4)
C4—C5—C6—O3	−130.9 (3)	C12—C13—C14—C9	48.8 (3)
C11—C5—C6—O3	113.1 (3)	C16—C13—C14—C9	−69.1 (3)
O2—C5—C6—C7	−136.0 (3)	C8—C9—C14—O7	−55.1 (3)
C4—C5—C6—C7	101.8 (3)	C10—C9—C14—O7	−172.4 (2)
C11—C5—C6—C7	−14.2 (3)	C8—C9—C14—C13	69.9 (3)
C25—O5—C7—C8	32.6 (3)	C10—C9—C14—C13	−47.3 (3)
C25—O5—C7—C17	153.2 (3)	O6—C8—C15—C16	−144.4 (3)
C25—O5—C7—C6	−89.4 (3)	C9—C8—C15—C16	−19.3 (4)
O3—C6—C7—O5	92.7 (3)	C7—C8—C15—C16	108.6 (3)
C5—C6—C7—O5	−145.3 (2)	C27—O8—C16—C15	155.1 (3)
O3—C6—C7—C8	−21.7 (4)	C27—O8—C16—C13	−81.3 (4)
C5—C6—C7—C8	100.2 (3)	C8—C15—C16—O8	144.4 (3)
O3—C6—C7—C17	−141.8 (3)	C8—C15—C16—C13	20.2 (4)
C5—C6—C7—C17	−19.9 (3)	C12—C13—C16—O8	155.7 (3)
C25—O6—C8—C9	159.4 (2)	C14—C13—C16—O8	−92.6 (3)
C25—O6—C8—C7	43.2 (3)	C12—C13—C16—C15	−86.1 (3)
C25—O6—C8—C15	−75.1 (3)	C14—C13—C16—C15	25.7 (4)
O5—C7—C8—O6	−46.9 (3)	C19—N1—C17—C11	−59.0 (3)
C17—C7—C8—O6	−171.3 (2)	C20—N1—C17—C11	170.3 (3)
C6—C7—C8—O6	73.4 (3)	C19—N1—C17—C7	53.9 (4)
O5—C7—C8—C9	−165.0 (2)	C20—N1—C17—C7	−76.8 (3)
C17—C7—C8—C9	70.6 (3)	C1—C11—C17—N1	−49.6 (3)
C6—C7—C8—C9	−44.8 (3)	C5—C11—C17—N1	69.7 (3)
O5—C7—C8—C15	65.4 (3)	C10—C11—C17—N1	−174.2 (2)
C17—C7—C8—C15	−59.0 (3)	C1—C11—C17—C7	−174.3 (3)
C6—C7—C8—C15	−174.3 (3)	C5—C11—C17—C7	−55.0 (3)
O6—C8—C9—C14	94.0 (3)	C10—C11—C17—C7	61.2 (3)
C7—C8—C9—C14	−157.4 (3)	O5—C7—C17—N1	49.7 (4)
C15—C8—C9—C14	−27.6 (4)	C8—C7—C17—N1	165.2 (3)
O6—C8—C9—C10	−153.1 (2)	C6—C7—C17—N1	−72.6 (3)
C7—C8—C9—C10	−44.6 (3)	O5—C7—C17—C11	169.0 (2)
C15—C8—C9—C10	85.3 (3)	C8—C7—C17—C11	−75.5 (3)
C8—C9—C10—C12	−92.5 (3)	C6—C7—C17—C11	46.8 (3)
C14—C9—C10—C12	26.5 (3)	C17—N1—C19—C4	42.6 (4)
C8—C9—C10—C11	35.9 (4)	C20—N1—C19—C4	174.0 (3)
C14—C9—C10—C11	154.9 (3)	C3—C4—C19—N1	77.9 (3)
O1—C1—C11—C17	−50.8 (3)	C18—C4—C19—N1	−162.8 (3)
C2—C1—C11—C17	70.8 (4)	C5—C4—C19—N1	−41.9 (4)
O1—C1—C11—C5	−162.5 (2)	C19—N1—C20—C21	70.1 (3)
C2—C1—C11—C5	−40.9 (4)	C17—N1—C20—C21	−157.8 (3)
O1—C1—C11—C10	75.3 (3)	C6—O3—C23—O4	−2.8 (5)
C2—C1—C11—C10	−163.1 (3)	C6—O3—C23—C24	176.8 (3)
O2—C5—C11—C17	165.9 (2)	C8—O6—C25—O5	−25.3 (3)
C6—C5—C11—C17	42.8 (3)	C7—O5—C25—O6	−5.7 (3)
C4—C5—C11—C17	−71.3 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O2—H2···O3	0.99 (5)	2.00 (5)	2.605 (3)	118 (4)
O2—H2···O9	0.99 (5)	2.13 (5)	2.936 (4)	138 (4)
C24—H24A···O9	0.98	2.53	3.427 (5)	153
C25—H25A···O2ⁱ	0.99	2.36	3.344 (4)	170

Symmetry code: (i) x−1, y, z.

Experimental details

Crystal data
Chemical formula	C₂₇H₄₁NO₈·C₃H₆O
M_r	565.69
Crystal system, space group	Orthorhombic, P2₁2₁2₁
Temperature (K)	120
a, b, c (Å)	8.4260 (8), 9.5546 (7), 35.237 (3)
V (Å³)	2836.8 (4)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.10
Crystal size (mm)	0.42 × 0.36 × 0.21

Data collection
Diffractometer	Oxford Diffraction Xcalibur Eos
Absorption correction	–
No. of measured, independent and observed [I > 2σ(I)] reflections	9839, 2930, 2690
R_int	0.022
(sin θ/λ)_max (Å⁻¹)	0.599

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.044, 0.104, 1.08
No. of reflections	2930
No. of parameters	373
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.69, −0.27

Computer programs: CrysAlis CCD (Oxford Diffraction, 2008), CrysAlis RED (Oxford Diffraction, 2008), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), OLEX2 (Dolomanov et al. 2009).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O2—H2···O3	0.99 (5)	2.00 (5)	2.605 (3)	118 (4)
O2—H2···O9	0.99 (5)	2.13 (5)	2.936 (4)	138 (4)
C24—H24A···O9	0.98	2.53	3.427 (5)	153
C25—H25A···O2ⁱ	0.99	2.36	3.344 (4)	170

Symmetry code: (i) x−1, y, z.

Acknowledgements

This project was supported by the Scientific Reseach Fund of Leshan Teachers' College, China (grant No. Z0975)

References

Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann, H. (2009). J. Appl. Cryst. 42, 339–341. Web of Science CrossRef CAS IUCr Journals Google Scholar
He, Y., Chen, D.-L. & Wang, F.-P. (2006). Nat. Prod. Commun. 5, 357–362. Google Scholar
Oxford Diffraction (2008). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Yarnton, England. Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Wang, F.-P., Chen, Q.-H. & Liu, X.-Y. (2009). The Alkaloids: Chemistry and Bioloy, Vol. 67, edited by G. A. Cordell, pp. 1–78. New York: Elsevier. Google Scholar