Phenylacetyl chloride → HCID 11617786, compound
Reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:13]2[O:17][C:16](=[O:18])[NH:15][N:14]=2)=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.[C:19]1([CH2:25][C:26](Cl)=[O:27])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[O:18]=[C:16]1[O:17][C:13]([C:4]2[S:3][C:2]([NH:1][C:26](=[O:27])[CH2:25][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[N:6][C:5]=2[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[N:14][NH:15]1Participants
3
Procedure
Prepared from 5-(2-amino-4-phenyl-thiazol-5-yl)-3H-[1,3,4]oxadiazol-2-one and phenyl-acetyl chloride.
Sources & evidence
- ORD record
- ord-f2bdfa4b89a6490dadead42a203356ef
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910613B2
Reaction notes
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