| Identification | More | [Name]
Dicyclopropane methylamine | [CAS]
13375-29-6 | [Synonyms]
AKOS MSC-0147
Dicyclopropane methylamine
DICYCLOPROPYL METHYL AMINE
1,1-Dicyclopropane methylamine
1,1-dicyclopropylmethanamine 1
1,1-DICYCLOPROPYLMETHANAMINE HYDROCHLORIDE
a-cyclopropylcyclopropanemethanamine
α-Cyclopropylcyclopropanemethanamine | [EINECS(EC#)]
236-451-7 | [Molecular Formula]
C7H17N | [MDL Number]
MFCD06804453 | [Molecular Weight]
115.22 | [MOL File]
13375-29-6.mol |
| Hazard Information | Back Directory | [Uses]
1,1-Dicyclopropylmethanamine is used as a reactant in the preparation of 4-dicyclopropylamino-7-aryl-7H-purines as CRF-1 antagonists with differentiated binding kinetic profiles. | [Synthesis]
General procedure for the synthesis of (dicyclopropylmethyl)amine from dicyclopropylketone oxime: In a 500 mL autoclave, 100 g of dicyclopropylketone oxime, 6 g of Ruanne nickel, 350 mL of water, and 10 g of sodium hydroxide were added in sequence. After replacing the air in the kettle with nitrogen three times, hydrogen was introduced. The hydrogen pressure of the reaction system was controlled to be 2 MPa, and the temperature was maintained at 70-80 °C for 4 hours. Upon completion of the reaction, the hydrogen pressure was released, the reaction mixture was cooled with continuous stirring, and the nickel catalyst in Nguyen was removed by filtration. The aqueous phase was extracted three times with 200 mL of dichloromethane, and the organic phases were combined and purified by distillation. Fractions from 100-110 °C were collected at a pressure of 100 mmHg to obtain the target product dicyclopropylmethylamine. About 81 g of product was finally obtained in 85.8% yield. | [References]
[1] Patent: CN104672093, 2016, B. Location in patent: Paragraph 0027-0028
[2] Synlett, 1999, # 4, p. 409 - 410
[3] Chemische Berichte, 1984, vol. 117, # 2, p. 856 - 858
[4] Helvetica Chimica Acta, 1963, vol. 46, p. 1059 - 1060
[5] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 1, p. 156 - 167 |
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