反应 #1884974

ord-4a965e8fa45c4fbeb1dc82ffd40d8848

反应方程式

C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)NS(=O)(=O)C1CC1
product
C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)NS(=O)(=O)C1CC1
cyclopropanesulfonic acid (1-(R)-tert-butoxycarbonylamino-2-(S)-vinylcyclopropanecarbonyl)-amide
ClCCl
dichloromethane
C=C[C@@H]1C[C@]1(N)C(=O)NS(=O)(=O)C1CC1.Cl
title compound
C=C[C@@H]1C[C@]1(N)C(=O)NS(=O)(=O)C1CC1.Cl
cyclopropanesulfonic acid (1-(R)-amino-2-(S)-vinyl-cyclopropanecarbonyl)amide HCl salt

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The volatiles were removed in vacuo
  2. 2
    浓缩concentrated in vacuo
  3. 3
    其他The resulting mixture was triturated from pentane
  4. 4
    过滤filtered

实验过程

A solution of the product of Step 2 (3.5 g, 10.6 mmol) in dichloromethane (35 mL) and TFA (32 mL) was stirred at room temperature for 1.5 hours. The volatiles were removed in vacuo and the residue suspended in 1N HCl in diethyl ether (20 mL) and concentrated in vacuo. This procedure was repeated once. The resulting mixture was triturated from pentane and filtered to give the title compound as a hygroscopic, off-white solid (2.60 g, 92%). 1H NMR: (DMSO-d6) 1.01-1.15 (m, 4H), 1.69-1.73 (m, 1H), 1.99-2.02 (m, 1H), 2.38 (q, J=9 Hz, 1H), 2.92-2.97 (m, 1H), 5.20 (d, J=11 Hz, 1H), 5.33 (d, J=17 Hz, 1H), 5.52-5.59 (m, 1H), 9.17 (br s, 3H); MS m/z 231 (M++H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08343477B2uspto-grants-2013_01