HCID 20297219, compound → HCID 178477388, compound
Reaction equation
[OH:1][C:2]1[CH:15]=[CH:14][C:5]([CH2:6][S:7]([CH:9]([CH3:13])[C:10]([OH:12])=O)=[O:8])=[CH:4][CH:3]=1.[NH2:16][CH:17]1[C:35](=[O:36])[N:19]2[C:20]([C:32]([OH:34])=[O:33])=[C:21]([CH:24]([S:26][C:27]3[NH:31][N:30]=[N:29][N:28]=3)[CH3:25])[CH2:22][S:23][C@H:18]12>>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][S:7]([CH:9]([CH3:13])[C:10]([NH:16][CH:17]2[C:35](=[O:36])[N:19]3[C:20]([C:32]([OH:34])=[O:33])=[C:21]([CH:24]([S:26][C:27]4[NH:28][N:29]=[N:30][N:31]=4)[CH3:25])[CH2:22][S:23][C@H:18]23)=[O:12])=[O:8])=[CH:14][CH:15]=1Participants
3
Procedure
456 mg. of 2-(p-hydroxybenzylsulfinyl)propionic acid and 7-amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid were reacted in the same manner as described in Example 28 and 291 mg. of 7-[2-(p-hydroxybenzylsulfinyl)propionamido]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid were obtained.
Sources & evidence
- ORD record
- ord-e4127867813945df9c4704d8e1975609
- Source dataset
- uspto-grants-1981_01
- Patent number
- US04245107
Reaction notes
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