[2-(4-Chloro-benzoylamino)-thiazol-4-yl]-acetic acid → HCID 59698853, compound
Reaction equation
[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]([NH:8][C:9]2[S:10][CH:11]=[C:12]([CH2:14][C:15]([OH:17])=O)[N:13]=2)=[O:7])=[CH:4][CH:3]=1.Cl.[CH3:21][S:22]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[C:31]1[CH:32]=[CH:33][C:34]([NH2:37])=[N:35][CH:36]=1)(=[O:24])=[O:23]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([NH:8][C:9]2[S:10][CH:11]=[C:12]([CH2:14][C:15](=[O:17])[NH:37][C:34]3[CH:33]=[CH:32][C:31]([C:26]4[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=4[S:22]([CH3:21])(=[O:24])=[O:23])=[CH:36][N:35]=3)[N:13]=2)=[O:7])=[CH:18][CH:19]=1Participants
3
Procedure
In analogy to example 1.3, [2-(4-chloro-benzoylamino)-thiazol-4-yl]-acetic acid (example 1.2) was coupled with 5-(2-methanesulfonyl-phenyl)-pyridin-2-ylamine, hydrochloride (CAS 209959-31-9) to give 4-chloro-N-(4-{[5-(2-methanesulfonyl-phenyl)-pyridin-2-ylcarbamoyl]-methyl}-thiazol-2-yl)-benzamide, using general procedure C. White solid. MS 527.2 ([M+H]+)
Sources & evidence
- ORD record
- ord-95a3404e8e474d1ba0c667594d1a2cb4
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07361672B2
Reaction notes
Loading…