Hydrochloric Acid → 7-[2-Carboxymethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-methylthiomethyl-3-cephem-4-carboxylic acid
Reaction equation
[C:1]([CH2:4][O:5][N:6]=[C:7]([C:26]1[N:27]=[C:28]([NH:31]C(=O)C(F)(F)F)[S:29][CH:30]=1)[C:8]([NH:10][CH:11]1[C:24](=[O:25])[N:13]2[C:14]([C:21]([OH:23])=[O:22])=[C:15]([CH2:18][S:19][CH3:20])[CH2:16][S:17][C@H:12]12)=[O:9])([OH:3])=[O:2].C([O-])(=O)C.[Na+].Cl>O>[C:1]([CH2:4][O:5][N:6]=[C:7]([C:26]1[N:27]=[C:28]([NH2:31])[S:29][CH:30]=1)[C:8]([NH:10][CH:11]1[C:24](=[O:25])[N:13]2[C:14]([C:21]([OH:23])=[O:22])=[C:15]([CH2:18][S:19][CH3:20])[CH2:16][S:17][C@H:12]12)=[O:9])([OH:3])=[O:2]Participants
5
Procedure
A solution of 7-[2-carboxymethoxyimino-2-{2-(2,2,2-trifluoroacetamido)thiazol-4-yl}acetamido]-3-methylthiomethyl-3-cephem-4-carboxylic acid (syn isomer) (4.1 g) and sodium acetate (9.56 g) in water (41 ml) was stirred for 19.5 hours at ambient temperature. The resultant solution was adjusted to pH 2.0 with conc. hydrochloric acid. The precipitates were collected by filtration and dried over phosphorus pentoxide to give 7-[2-carboxymethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-methylthiomethyl-3-cephem-4-carboxylic acid (syn isomer) (1.8 g), mp 173°-176° C. (dec.).
Workup
- filtrationThe precipitates were collected by filtration
- dry with materialdried over phosphorus pentoxide
Sources & evidence
- ORD record
- ord-8e5035f4a23f4fc7839f85059072dbb8
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04409215
Reaction notes
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