7-[2-Ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate acetone → 7-[2-Ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate
Reaction equation
CC(C)=O.[CH2:5]([O:7][N:8]=[C:9]([C:32]1[N:36]=[C:35]([NH2:37])[S:34][N:33]=1)[C:10]([NH:12][CH:13]1[C:30](=[O:31])[N:15]2[C:16]([C:27]([O-:29])=[O:28])=[C:17]([CH2:20][N+:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH2:18][S:19][C@H:14]12)=[O:11])[CH3:6]>O>[CH2:5]([O:7][N:8]=[C:9]([C:32]1[N:36]=[C:35]([NH2:37])[S:34][N:33]=1)[C:10]([NH:12][CH:13]1[C:30](=[O:31])[N:15]2[C:16]([C:27]([O-:29])=[O:28])=[C:17]([CH2:20][N+:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH2:18][S:19][C@H:14]12)=[O:11])[CH3:6]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate acetone adduct (syn isomer)(1.0 g) in water (1 ml) was stood on for 5 days in a freezer at -20° C. A mixture of ice and precipitates was stood on at ambient temperature until the ice was melted. The resulting precipitates were collected by filtration, washed with water (0.3 ml) and dried in vacuo to give 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate (syn isomer)(0.52 g) as colorless needles, mp 165° to 170° C. (dec.).
Workup
- customwas stood on for 5 days in a freezer at -20° C
- additionA mixture of ice
- customprecipitates
- customwas stood on at ambient temperature until the ice
- customThe resulting precipitates
- filtrationwere collected by filtration
- washwashed with water (0.3 ml)
- customdried in vacuo
Sources & evidence
- ORD record
- ord-4e442d1db119444090fdb1d02564cc82
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04408042
Reaction notes
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