HCID 54083585, compound → HCID 131713974, compound
Reaction equation
[Cl:1][CH2:2][C:3]([NH:5][C:6]1[S:7][CH:8]=[C:9]([C:11](=[N:15][O:16][CH2:17][CH3:18])[C:12]([OH:14])=O)[N:10]=1)=[O:4].[NH2:19][CH:20]1[C:46](=[O:47])[N:22]2[C:23]([C:30]([O:32][CH:33]([C:40]3[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=3)[C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)=[O:31])=[C:24]([CH2:27][O:28][CH3:29])[CH2:25][S:26][C@H:21]12>>[Cl:1][CH2:2][C:3]([NH:5][C:6]1[S:7][CH:8]=[C:9]([C:11](=[N:15][O:16][CH2:17][CH3:18])[C:12]([NH:19][CH:20]2[C:46](=[O:47])[N:22]3[C:23]([C:30]([O:32][CH:33]([C:40]4[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=4)[C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=4)=[O:31])=[C:24]([CH2:27][O:28][CH3:29])[CH2:25][S:26][C@H:21]23)=[O:14])[N:10]=1)=[O:4]Participants
3
Procedure
Following the method of Preparation 3, 225 mg of 2-(2-chloroacetamidothiazol-4-yl)-2-ethoxyiminoacetic acid and 200 mg of benzhydryl 7-amino-3-methoxymethyl-3-cephem-4-carboxylate were reacted to give 280 mg of benzhydryl 7-[2-(2-chloroacetamidothiazol-4-yl)-2-ethoxyiminoacetamido]-3-methoxymethyl-3-cephem-4-carboxylate, in the form of a yellow powder.
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-5a179ccfa1a34759a38d8f744ec57fb6
- Source dataset
- uspto-grants-1984_12
- Patent number
- US04486425
Reaction notes
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