反応式
[C:1]1([CH2:7][C:8]([NH:10][C@H:11]([C:13]([OH:15])=O)[CH3:12])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:16][CH:17]1[CH2:24][CH2:23][CH2:22][NH:21][C:19](=[O:20])[CH2:18]1>>[C:1]1([CH2:7][C:8]([NH:10][C@H:11]([C:13]([NH:16][CH:17]2[CH2:24][CH2:23][CH2:22][NH:21][C:19](=[O:20])[CH2:18]2)=[O:15])[CH3:12])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1参加物
3
実験手順
Following General Procedure B above using N-(phenylacetyl)-L-alanine (Example A) and 3-aminocaprolactam (Sigma), the title compound was prepared as a solid having a melting point of 200-202° C. The reaction was monitored by tlc on silica gel (Rf=0.30 in 1:9 methanol/dichloromethane).
出典と根拠
- ORDレコード
- ord-987c3041d8ff4f4fa979fdca053d055a
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07390801B2
関連ノート
読み込み中…