[2-(2-Dibenzylamino-ethoxy)-ethyl]methyl-carbamic acid tert-butyl ester → tert-butyl N-(2-(2-aminoethoxy)ethyl)-N-methylcarbamate
反応式
[C:1]([O:5][C:6](=[O:29])[N:7]([CH2:9][CH2:10][O:11][CH2:12][CH2:13][N:14](CC1C=CC=CC=1)CC1C=CC=CC=1)[CH3:8])([CH3:4])([CH3:3])[CH3:2]>CO.[Pd]>[C:1]([O:5][C:6](=[O:29])[N:7]([CH2:9][CH2:10][O:11][CH2:12][CH2:13][NH2:14])[CH3:8])([CH3:4])([CH3:2])[CH3:3]参加物
4
実験手順
[2-(2-Amino-ethoxy)-ethyl]-methyl-carbamic acid tert-butyl ester (100 mg) was prepared following General Procedure T starting from [2-(2-dibenzylamino-ethoxy)-ethyl]-methyl-carbamic acid tert-butyl ester (200 mg) and Pd—C (40 mg) in methanol (1.5 mL).
出典と根拠
- ORDレコード
- ord-3bcd6dd6aaa54ab5aa47ded7783c635f
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08759535B2
反応ノート
読み込み中…