반응 #49075

ord-4bf2fb03e43e4c53a873d58806566f7a

반응 방정식

[BH4-].[Na+]
sodium borohydride
CC(C)(C#N)N1CC2CC2C1
2-(3-azabicyclo[3.1.0]hex-3-yl)-2-methylpropanenitrile
[Li][c]1ccccc1
phenyllithium
CN(C)C1(C(N)c2ccccc2)CCCC1
D2
CN(C)C1(C(N)c2ccccc2)CCCC1
Racemic {1-[amino(phenyl)methyl]cyclopentyl}dimethylamine
CC(C)(C(N)c1ccccc1)N1CC2CC2C1
title compound
수율 44.0%
CC(C)(C(N)c1ccccc1)N1CC2CC2C1
(±)2-(3-Azabicyclo[3.1.0]hex-3-yl)-2-methyl-1-phenyl-1-propanamine
수율 44.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound (393 mg, 44%) was prepared from 2-(3-azabicyclo[3.1.0]hex-3-yl)-2-methylpropanenitrile D15 (583 mg, 3.9 mmol), and phenyllithium in dibutylether (2.15 ml of a 2.0M solution; 4.3 mmol) in THF (7 ml), followed by reaction with sodium borohydride (445 mg, 11.7 mmol) in methanol (10 ml) in a similar manner to that described in D2. 1H NMR (CDCl3) δ: 0.38 (1H, m), 0.66 (1H, m), 0.74 (3H, s), 0.93 (3H, s), 1.30-1.40 (2H, m), 1.74 (2H, bs), 2.67 (2H, m), 2.91 (2H, t, J=8 Hz), 4.03 (1H, s), 7.20-7.30 (3H, m), 7.38 (2H, m).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745642B2uspto-grants-2010_06