Hydrochloric Acid → HCID 178429635, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([C:7](=[N:24][O:25][CH2:26][C:27]([OH:29])=[O:28])[C:8]([NH:10][CH:11]2[C:22](=[O:23])[N:13]3[C:14]([C:19]([OH:21])=[S:20])=[C:15]([CH3:18])[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1.[ClH:30]>O>[ClH:30].[NH2:1][C:2]1[S:3][CH:4]=[C:5]([C:7](=[N:24][O:25][CH2:26][C:27]([OH:29])=[O:28])[C:8]([NH:10][CH:11]2[C:22](=[O:23])[N:13]3[C:14]([C:19]([OH:21])=[S:20])=[C:15]([CH3:18])[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 7-[2-(2-aminothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-methylthio-3-cephem-4-carboxylic acid (syn isomer) (10 g) in water (80 ml) was added dropwise conc. hydrochloric acid (10 ml) at room temperature under stirring and the mixture was stirred at the same temperature for one hour. The precipitates were filtered and washed with cold water and dried to give 7-[2-(2-aminothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-methylthio-3-cephem-4-carboxylic acid hydrochloride (syn isomer) (9.5 g).
Workup
- stirringthe mixture was stirred at the same temperature for one hour
- filtrationThe precipitates were filtered
- washwashed with cold water
- customdried
Sources & evidence
- ORD record
- ord-483cdfcc42cc45f381d4d1b84e042aa6
- Source dataset
- uspto-grants-1984_06
- Patent number
- US04452851
Reaction notes
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