2-Amino-4,5,6,7-tetrahydrobenzothiazole → 5-chloro-2-methoxy-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)benzamide

HRID 1037922

反応式

HRID 1037922 の反応式
[S:1]1[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=2[N:3]=[C:2]1[NH2:10].[Cl:11][C:12]1[CH:13]=[CH:14][C:15]([O:21][CH3:22])=[C:16]([CH:20]=1)[C:17](O)=[O:18]>>[Cl:11][C:12]1[CH:13]=[CH:14][C:15]([O:21][CH3:22])=[C:16]([CH:20]=1)[C:17]([NH:10][C:2]1[S:1][C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=2[N:3]=1)=[O:18]

参加物

3

反応物 2

HCID 180462-Amino-4,5,6,7-tetrahydrobenzothiazoleHCID 769705-Chloro-o-anisic acid

生成物 1

HCID 8879545-chloro-2-methoxy-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)benzamide

実験手順

Commercially available 4,5,6,7-tetrahydrobenzo[d]thiazol-2-amine (Aldrich) and 5-chloro-2-methoxybenzoic acid (Aldrich) were processed using the method described in Example 58 to afford the title compound MS (ESI+) m/z 323 (M+H)+.

出典と根拠

ORDレコード
ord-6dbd5fe01a91402eb922745f96586384
出典データセット
uspto-grants-2013_10
特許番号
US08546583B2

関連ノート

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