反応 #1583826

ord-d2c6227684bf4edea1dc63c49057823b

反応方程式

COC(=O)NCc1cc(C(=O)C=CN(C)C)ccc1Cl
methyl N-[[2-chloro-5-[3-(dimethylamino)-1-oxo-2-propen-1-yl]phenyl]methyl]carbamate
COC(=O)NCc1cc(C(=O)C=CN(C)C)ccc1Cl
product
COC(=O)NCc1cc(C(=O)C=CN(C)C)ccc1Cl
methyl N-[[2-chloro-5-[3-(dimethylamino)-1-oxo-2-propen-1-yl]phenyl]methyl]carbamate
NN.O
hydrazine hydrate
COC(=O)NCc1cc(-c2cc[nH]n2)ccc1Cl
title compound
COC(=O)NCc1cc(-c2cc[nH]n2)ccc1Cl
methyl N-[[2-chloro-5-(1H-pyrazol-3-yl)phenyl]methyl]carbamate

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction mixture was filtered
  2. 2
    その他the solid collected
  3. 3
    その他was dried under reduced pressure

実験手順

To a solution of methyl N-[[2-chloro-5-[3-(dimethylamino)-1-oxo-2-propen-1-yl]phenyl]methyl]carbamate (i.e. the product of Step A) (4.14 g, 13.9 mmol) in methanol (80 mL) was added hydrazine hydrate (0.771 g, 15.4 mmol). The reaction mixture was stirred at room temperature for 2 days. The reaction mixture was filtered and the solid collected was dried under reduced pressure to provide the title compound, a compound of the present invention, as a solid (3.26 g).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09198433B2uspto-grants-2015_12