Home Physical Sciences Crystal structure of 8-isopropyl-8-aza-bicyclo[3.2.1]octan-3-ol, C10H19NO
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Crystal structure of 8-isopropyl-8-aza-bicyclo[3.2.1]octan-3-ol, C10H19NO

  • Xiao-Li Yang EMAIL logo and Kun-Yan Wang
Published/Copyright: September 17, 2016

Abstract

C10H19NO, monoclinic, P21/c (no. 14), a = 6.2427(16) Å, b = 9.553(2) Å, c = 16.932(4) Å, β = 100.094(7)°, V = 994.1(4) Å3, Z = 4, Rgt(F) = 0.060, wRref(F2) = 0.094, T = 296(2) K.

CCDC no.:: 1501346

Table 1

Data collection and handling.

Crystal:Colourless blocks Size 0.27 × 0.20 × 0.16 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.7 cm−1
Diffractometer, scan mode:Nonius CAD4, ω/2θ
2θmax, completeness:50.8°, >98%
N(hkl)measured, N(hkl)unique, Rint:5669, 1826, 0.108
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 923
N(param)refined:114
Programs:CAD4 programs [4, 5], SHELX [6]
Table 2

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

AtomxyzUiso*/Ueq
C1−0.0607(3)0.6121(2)0.30990(12)0.0374(6)
H1−0.18300.67080.31880.045*
C2−0.0811(4)0.4647(2)0.34465(14)0.0483(7)
H2A−0.16260.46730.38840.058*
H2B−0.15240.40110.30370.058*
C30.1556(3)0.4204(2)0.37460(14)0.0465(7)
H3A0.19010.33520.34830.056*
H3B0.18240.40560.43220.056*
C40.2893(3)0.5443(2)0.35190(13)0.0391(6)
H40.42420.55410.39100.047*
C50.3398(3)0.5354(2)0.26742(13)0.0422(6)
H5A0.41860.61900.25700.051*
H5B0.43440.45580.26440.051*
C60.1397(4)0.5210(2)0.20244(13)0.0420(6)
H60.17660.55240.15140.050*
C7−0.0448(3)0.6102(2)0.22151(12)0.0407(6)
H7A−0.18070.57540.19130.049*
H7B−0.02550.70530.20400.049*
C80.1260(4)0.7108(2)0.43824(14)0.0502(7)
H80.06300.63230.46360.060*
C9−0.0242(4)0.8355(3)0.43603(15)0.0773(9)
H9A0.03510.91310.41090.116*
H9B−0.03840.86070.48980.116*
H9C−0.16460.81200.40600.116*
C100.3445(4)0.7468(3)0.48856(14)0.0825(10)
H10A0.43360.66430.49640.124*
H10B0.32320.78220.53970.124*
H10C0.41520.81670.46150.124*
N10.1473(3)0.66905(16)0.35503(10)0.0346(5)
O10.0651(3)0.37937(16)0.19364(10)0.0536(5)
H1A0.175(3)0.330(2)0.1836(13)0.064*

The asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details of the measurement method and a list of the atoms including atomic coordinates and displacement parameters.

Source of material

The compound we report is easily available by a literature known synthesis [1]. In a 500 mL three-neck flask, a mixture of 2,5-dimethoxy-tetrahydrofuran (50 g, 378.3 mmol) and HCl (33%, 170 mL) was stirred at reflux temperature for 3 h. Then isopropylamine hydrochloride (43.4 g, 453.96 mmol) and sodium acetate (31 g, 378.3 mmol) was added. Finally, 1,3-acetonedicarboxylic acid (55.27 g, 378.3 mmol) was added and the reaction was stirred for another 3 h. After completion the mixture was cooled to room temperature, potassium carbonate was added, and saturated with sodium chloride. Then it was filtered at room temperature and extracted with chloroform (100 mL) for five times. Organic phases were combined and concentrated yielding N-isopropylnortropinone (57.53 g, 91%).

In a hydrogenation reactor N-isopropylnortropinone (57.53 g, 343.98 mmol), Raney-Ni (1 g) and ethanol (500 mL, 95%) were added, the air was exchanged with hydrogen for three times. Then hydrogen was added to a pressure of 2 MPa and the reaction was continued for 5 h. After completion of the reaction, it was cooled to room temperature, the reaction system was filtered and concentrated. The crude N-isopropylnortropine (57.06 g, 98%) was obtained as brown solid. Then 0.5 g of the title compound was dissolved in 5 mL ethanol solution. Evaporation at room temperature yielded colourless crystals.

Experimental details

The hydrogen atoms were placed on calculated positions with the help of the SHELX program [6].

Discussion

The title compound N-isopropylnortropine is a Noratropine derivative and is known as an important intermediate in the production of ipratropium bromide [2].

There is one molecule in the asymmetric unit of the title structure. All bond lengths and bond angles are in the normal ranges [3].

In the molecule the plane formed by C1, C2, C3 and C4 and C1, C4, C7 and C5 are nearly flat.

There is an intermolecular OH⋯N hydrogen bond which connects adjacent molecules into an one-dimensional chain along the b direction.

Acknowledgements:

This work was financially supported by Research Fund for the Doctoral Program of Jinling Institute of Technology (jit-2012-27), the Natural Science Foundation of China (Grant numbers 51103071).

References

1. Tsyskovskaia, I.; Kandil, M.; Beaumier, Y.: Synthesis of ipratropium bromide-related compounds. Synth. Commun. 37 (2007) 439–446.10.1080/00397910601039119Search in Google Scholar

2. Bauer, R.; Kuhn, F.; Stockhaus, K.; Wiek, H.: Allgemeine Pharmakologie und seckretionshemmende Wirkung von (8r)-3α-Hydroxy-8-isopropyl-1αH,5αH-tropaniumbromid-()tropat (Ipratropiumbromid) Arzneim-Forsch. 26 (1976) 974–980.Search in Google Scholar

3. Allen, F. H.; Kennard, O.; Watson, D. G.; Brammer, L.; Orpen, A. G.; Taylor, R.: Tables of bond lengths determined by X-ray and neutron diffraction. Part 1. Bond lengths in organic compounds. J. Chem. Soc. Perkin Trans. 2 (1987) S1–S19.10.1039/p298700000s1Search in Google Scholar

4. Enraf-Nonius: CAD-4 Software. Version 5.0. Enraf-Nonius, Delft, The Netherlands, 1985.Search in Google Scholar

5. Harms, K.; Wocadlo, S.: XCAD4. University of Marburg, Germany, 1995.Search in Google Scholar

6. Sheldrick, G. M.: A short history of SHELX. Acta Crystallogr. A64 (2008) 112–122.10.1107/S0108767307043930Search in Google Scholar PubMed

Received: 2016-5-4
Accepted: 2016-8-29
Published Online: 2016-9-17
Published in Print: 2016-12-1

©2016 Xiao-Li Yang et al., published by De Gruyter.

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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  73. Crystal structure of 4-(4-((3-bromophenyl)amino)-6-(tert-butyl)-3-(2-hydroxypropan-2-yl)cinnolin-8-yl)-2-methylbut-3-yn-2-ol, C26H30BrN3O2
  74. Crystal structure poly-(μ2-1-(4-(1H-imidazol-1-yl)benzyl)-1H-1,2,4-triazolyl-κ2NN1:N2N)-(μ3-2,2′-(1,2-phenylene)diacetato-κ5-O1,O2:O2:O3,O4)cadmium(II), C22H19CdN5O4
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  76. Redetermination of the crystal structure of potassium lithium molybdate monohydrate, KLiMoO4·H2O
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