1-Isocyanato-2-phenoxybenzene → (S)-Methyl 3-methyl-2-(1-oxo-6-(4-(3-(2-phenoxyphenyl)ureido)phenyl)isoindolin-2-yl)butanoate

HRID 403730ノート

反応式

HRID 403730 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:16]=[C:15]3[C:11]([CH2:12][N:13]([C@@H:18]([CH:23]([CH3:25])[CH3:24])[C:19]([O:21][CH3:22])=[O:20])[C:14]3=[O:17])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[O:26]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=1[N:39]=[C:40]=[O:41])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH3:24][CH:23]([CH3:25])[C@H:18]([N:13]1[CH2:12][C:11]2[C:15](=[CH:16][C:8]([C:5]3[CH:4]=[CH:3][C:2]([NH:1][C:40]([NH:39][C:34]4[CH:35]=[CH:36][CH:37]=[CH:38][C:33]=4[O:26][C:27]4[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=4)=[O:41])=[CH:7][CH:6]=3)=[CH:9][CH:10]=2)[C:14]1=[O:17])[C:19]([O:21][CH3:22])=[O:20]

参加物

3

反応物 2

HCID 27333891-Isocyanato-2-phenoxybenzeneHCID 131731441(S)-Methyl 2-(6-(4-aminophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoate

生成物 1

HCID 123397814(S)-Methyl 3-methyl-2-(1-oxo-6-(4-(3-(2-phenoxyphenyl)ureido)phenyl)isoindolin-2-yl)butanoate収率 98%

実験手順

The compound of example 47 was prepared analogous to compound of example 7 by reaction of compound of example 6 with 2-phenoxy phenyl isocyanate.

出典と根拠

ORDレコード
ord-18b4dedb078f4d9c9e362e75cfc0e224
出典データセット
uspto-grants-2014_06
特許番号
US08748426B2

反応ノート

読み込み中…