Hydrochloric Acid → HCID 178460189, compound
Reaction equation
C([NH:3][C:4]1[S:5][CH:6]=[C:7]([C:9](=[N:35][O:36][CH2:37][CH:38]=[CH2:39])[C:10]([NH:12][CH:13]2[C:33](=[O:34])[N:15]3[C:16]([C:30]([OH:32])=[O:31])=[C:17]([CH:20]([S:24][C:25]4[NH:29][N:28]=[N:27][N:26]=4)[CH2:21][CH2:22][OH:23])[CH2:18][S:19][C@H:14]23)=[O:11])[N:8]=1)=O.[ClH:40]>>[ClH:40].[NH2:3][C:4]1[S:5][CH:6]=[C:7]([C:9](=[N:35][O:36][CH2:37][CH:38]=[CH2:39])[C:10]([NH:12][CH:13]2[C:33](=[O:34])[N:15]3[C:16]([C:30]([OH:32])=[O:31])=[C:17]([CH:20]([S:24][C:25]4[NH:29][N:28]=[N:27][N:26]=4)[CH2:21][CH2:22][OH:23])[CH2:18][S:19][C@H:14]23)=[O:11])[N:8]=1Participants
3
Procedure
7-[2-(2-Formamidothiazol-4-yl)-2-allyloxyiminoacetamido]-3-[1-(2-hydroxyethyl)-1H-tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid (syn isomer, 2.7 g) was treated with conc. hydrochloric acid (0.94 g) in a similar manner to that of Example 1-(2) to give 7-[2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetamido]-3-[1-(2-hydroxyethyl)-1H tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid hydrochloride (syn isomer, 2.72 g).
Sources & evidence
- ORD record
- ord-04dfe25bd3054b8080dfd09bb4670316
- Source dataset
- uspto-grants-1982_12
- Patent number
- US04366153
Reaction notes
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