Benzoyl chloride → HCID 11157476, compound
Reaction equation
[O:1]([C:8]1[CH:15]=[CH:14][C:11]([CH2:12][NH2:13])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[CH2:17][C:18]1[S:19][CH:20]=[C:21]([C:23](Cl)=[O:24])[N:22]=1.[C:26](Cl)(=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.[NH2:35][C:36]1[CH:48]=[CH:47][C:39]2[O:40]C(C)(C)[O:42][C:43](=[O:44])[C:38]=2[CH:37]=1>>[C:26]([N:35]([CH2:17][C:18]1[S:19][CH:20]=[C:21]([C:23]([NH:13][CH2:12][C:11]2[CH:10]=[CH:9][C:8]([O:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[CH:15][CH:14]=2)=[O:24])[N:22]=1)[C:36]1[CH:48]=[CH:47][C:39]([OH:40])=[C:38]([CH:37]=1)[C:43]([OH:44])=[O:42])(=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1Participants
5
Procedure
The title compound was prepared following the procedure A using 4-phenoxybenzylamine, 2-(chloromethyl)-1,3-thiazole-4-carbonyl chloride, benzoyl chloride and 6-amino-2,2-dimethyl-4H-1,3-benzodioxin-4-one. M+(ESI): 580.9
Sources & evidence
- ORD record
- ord-e120ed6ab5434d0fbe8ba9b3a31f088f
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365225B2
Reaction notes
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