Propionyl chloride → N-(1H-pyrrolo[3,2-c]pyridin-4-yl)propanamide
反応式
NC1C2C=CN(C(OCC3C=CC=CC=3)=O)C=2C=CN=1.C(Cl)(=O)CC.[NH:26]1[C:34]2[CH:33]=[CH:32][N:31]=[C:30]([NH:35][C:36]([CH:38]3C[CH2:39]3)=[O:37])[C:29]=2[CH:28]=[CH:27]1>>[NH:26]1[C:34]2[CH:33]=[CH:32][N:31]=[C:30]([NH:35][C:36](=[O:37])[CH2:38][CH3:39])[C:29]=2[CH:28]=[CH:27]1参加物
4
実験手順
This was prepared by treating benzyl 4-amino-1H-pyrrolo[3,2-c]pyridine-1-carboxylate with propionyl chloride following a procedure similar to the one described herein. for intermediate 28.
後処理
- customThis was prepared
出典と根拠
- ORDレコード
- ord-67be5d4cbd904e6ba1bada483cd889b7
- 出典データセット
- uspto-grants-2016_06
- 特許番号
- US09364466B2
反応ノート
読み込み中…