Chloroacetyl chloride → HCID 19352176, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)=[CH:4][CH:3]=1.[Cl:17]CC(Cl)=O.[Cl:22][CH2:23][C:24](NC1C=CC(C2SC3C=CC=CC=3N=2)=CC=1)=[O:25]>C1C=CC=CC=1>[ClH:17].[Cl:22][CH2:23][C:24]([NH:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)=[CH:6][CH:7]=1)=[O:25]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(4'-Aminophenyl)benzoxazole (0.28 g, 1.33 mmol) was treated with chloroacetyl chloride (0.5 ml) in benzene (15 ml) according to the procedure described above for preparation of 2-(4'-chloroacetamidophenyl)benzothiazole. 2-(4'-Chloroacetamidophenyl)benzoxazole hydrochloride was obtained (0.31 g, 72%).
Sources & evidence
- ORD record
- ord-65420691235d4d3f95025ab355bdcbe8
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06034246
Reaction notes
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