2-Ethoxybenzoyl chloride → 1-(2-Ethoxy-benzoyl)-pyrrolidine-3-carboxylic acid ethyl ester
反応式
[CH2:1]([O:3][C:4]([CH:6]1[CH2:10][CH2:9][NH:8][CH2:7]1)=[O:5])[CH3:2].[CH2:11]([O:13][C:14]1[CH:22]=[CH:21][CH:20]=[CH:19][C:15]=1[C:16](Cl)=[O:17])[CH3:12]>>[CH2:1]([O:3][C:4]([CH:6]1[CH2:10][CH2:9][N:8]([C:16](=[O:17])[C:15]2[CH:19]=[CH:20][CH:21]=[CH:22][C:14]=2[O:13][CH2:11][CH3:12])[CH2:7]1)=[O:5])[CH3:2]参加物
3
実験手順
The title compound was prepared according to the method described for Preparation 2 using pyrrolidine-3-carboxylic acid ethyl ester (see Preparation 1) and 2-ethoxy-benzoyl chloride to afford the title compound as a pale yellow oil (5.13 g, 83%).
後処理
- customThe title compound was prepared
出典と根拠
- ORDレコード
- ord-5e77c7e39a32448e9f3d159b16158cc4
- 出典データセット
- uspto-grants-2012_10
- 特許番号
- US08278343B2
反応ノート
読み込み中…