Hydrochloric Acid → HCID 178514096, compound
Reaction equation
[Na+].[C:2]([NH:12][CH:13]1[C:36](=[O:37])[N:15]2[C:16]([C:33]([O-:35])=[O:34])=[C:17]([CH:20]([S:27][C:28]3[NH:32][N:31]=[N:30][N:29]=3)[CH2:21][CH2:22][NH:23][C:24]([NH2:26])=[O:25])[CH2:18][S:19][C@H:14]12)(=[O:11])[C@@H:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[OH:4].Cl>>[C:2]([NH:12][CH:13]1[C:36](=[O:37])[N:15]2[C:16]([C:33]([OH:35])=[O:34])=[C:17]([CH:20]([S:27][C:28]3[NH:32][N:31]=[N:30][N:29]=3)[CH2:21][CH2:22][NH:23][C:24]([NH2:26])=[O:25])[CH2:18][S:19][C@H:14]12)(=[O:11])[C@@H:3]([C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)[OH:4]Participants
3
Procedure
An aqueous solution of 7-D-mandelamido-3-[1-(2-ureidoethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid sodium salt is acidified with 3 N HCl to pH 2.5 and extracted with ethyl acetate. The extract is dried over anhydrous magnesium sulfate and evaporated to dryness to give the title compound.
Workup
- extractionextracted with ethyl acetate
- dry with materialThe extract is dried over anhydrous magnesium sulfate
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-363cf8db52544609be278677adb61338
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04066761
Reaction notes
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