反応 #1884970

ord-c1ac1dcdfce940458d5073160d82ee97

反応方程式

CC(C)(C)NC(=O)O.COCC1(S(N)(=O)=O)CC1
1-methoxymethylcyclopropylsulfonylamine tert-butyl-carbamate
CCCN=C=O
n-propyl isocyanate
CC(C)(C)NC(=O)O.CCCNC(=O)C1(S(N)(=O)=O)CC1
1-propylcarbamoylcyclopropanesulfonamide tert-butylcarbamate
収率 100.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他This compound was obtained in a crude 100% yield
  2. 2
    その他The compound was taken directly into the next reaction without purification

実験手順

This compound was obtained in a crude 100% yield according to the procedure described for the synthesis of 1-methoxymethylcyclopropylsulfonylamine tert-butyl-carbamate except that 1.10 equivalents of n-propyl isocyanate was used as the electrophile. The compound was taken directly into the next reaction without purification: 1H NMR (CDCl3) δ 0.10 (m, 2H), 0.51 (m, 2H), 0.67 (m, 1H), 1.10 (m, 2H), 1.49 (s, 9H), 1.62 (m, 2H), 1.87 (d, J=7.0 Hz, 2H).

出典

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