Phenoxyacetyl chloride → HCID 70562397, compound
Reaction equation
[NH2:1][CH:2]1[C:26](=[O:27])[N:4]2[C:5]([C:10]([O:12][CH:13]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[O:11])=[C:6]([Br:9])[CH2:7][S:8][C@H:3]12.[O:28]([CH2:35][C:36](Cl)=[O:37])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>N1C=CC=CC=1>[O:28]([CH2:35][C:36]([NH:1][CH:2]1[C:26](=[O:27])[N:4]2[C:5]([C:10]([O:12][CH:13]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[O:11])=[C:6]([Br:9])[CH2:7][S:8][C@H:3]12)=[O:37])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Diphenylmethyl 7-amino-3-bromo-3-cephem-4-carboxylate is reacted with phenoxyacetyl chloride in the presence of pyridine to provide diphenylmethyl 7-phenoxyacetamido-3-bromo-3-cephem-4-carboxylate.
Sources & evidence
- ORD record
- ord-43acc3b9e8a242e4b83c84819a3af9c0
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03962227
Reaction notes
Loading…