Реакция #969890

ord-52867257580c4af0bf082b8a3e028a37

Уравнение реакции

CS(=O)(=O)Cl
methane sulfonyl chloride
CCc1ccc(CCO)nc1
2-(5-ethyl-pyridine-2-yl)-ethanol
CCN(CC)CC
triethylamine
CS(=O)(=O)Cl
methane sulfonyl chloride
CCc1ccc(CCOS(C)(=O)=O)nc1
title compound
CCc1ccc(CCOS(C)(=O)=O)nc1
Methanesulfonic acid 2-(5-ethyl-pyridin-2-yl)-ethyl ester

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe reaction stirred for 30 min
  2. 2
    Промывкаwashed with H2O and brine
  3. 3
    СушкаThe organic layer was dried (MgSO4)
  4. 4
    Концентрированиеthe solution concentrated

Методика

To a solution of 2-(5-ethyl-pyridine-2-yl)-ethanol (25.34 g) and triethylamine (46.7 mL) in DCM (130 mL) at 0° C. under nitrogen was added methane sulfonyl chloride (15.56 mL), then the reaction mixture was allowed to warm to room temperature and stirred overnight. A further portion of methane sulfonyl chloride (3.88 mL) was added and the reaction stirred for 30 min. The reaction was diluted with DCM and washed with H2O and brine. The organic layer was dried (MgSO4) and the solution concentrated to give the title compound as a red oil (38.24 g). 1H NMR (400 MHz, CDCl3): δ 8.39 (d, J=2.2 Hz, 1H), 7.47 (dd, J=7.7, 2.3 Hz, 1H), 7.14 (d, J=7.7 Hz, 1H), 4.64 (t, J=6.5 Hz, 2H), 3.19 (t, J=6.5 Hz, 2H), 2.90 (s, 3H), 2.64 (q, J=7.6 Hz, 2H), 1.25 (t, J=7.6 Hz, 3H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08236786B2uspto-grants-2012_08