Реакция #58604

ord-1638e1e420454f05a48fbbf6f0f6cc7c

Уравнение реакции

OC(Cc1ccccc1-c1ccccc1)(C1CCCC1)C1CN(Cc2ccccc2)CCO1
47
OC(Cc1ccccc1-c1ccccc1)(C1CCCC1)C1CN(Cc2ccccc2)CCO1
2-[1,1′-Biphenyl]-2-yl-1-cyclopentyl-1-[4-(phenylmethyl)morpholin-2-yl]ethanol
CCN(C(C)C)C(C)C
Hünig's base
CC(Cl)OC(=O)Cl
α-chloroethyl chloroformate
Cl.OC(Cc1ccccc1-c1ccccc1)(C1CCCC1)C1CNCCO1
48
Cl.OC(Cc1ccccc1-c1ccccc1)(C1CCCC1)C1CNCCO1
2-[1,1′-Biphenyl]-2-yl-1-cyclopentyl-1-morpholin-2-ylethanol hydrochloride

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеPurification by ion exchange chromatography

Методика

The free base of 48 is prepared from 47 (1.75 g, 3.95 mmol), solid supported Hünig's base (2.22 g) and α-chloroethyl chloroformate (1.62 mL) in anhydrous DCM (30 mL) following General Procedure 3. Purification by ion exchange chromatography followed by flash column chromatography (eluent, MeOH/DCM 1/99 to 20/80 [v/v]) gives the free base as a viscous oil (805 mg, 58%) which is converted into 48 following General Procedure 4. MW 387.95; C23H29NO2.HCl; 1H NMR (CD3OD): δ 7.66-7.40 (1H, m) 7.19-7.47 (8H, m), 3.92 (1H, dd, 13 Hz, 3.5 Hz), 3.59-3.67 (2H, m), 3.05-3.16 (4H, m), 2.93 (1H, td, 13 Hz, 3.5 Hz,), 2.59 (1H, t, 12 Hz), 1.98-1.88 (1H, m), 1.55-1.19 (8H, m); LCMS: (12 minute method) m/z 351 [M−HCl+H]+, RT 5.68 min.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07423037B2uspto-grants-2008_09