Hydrochloric Acid → 7-[2-Carboxymethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-methylthiomethyl-3-cephem-4-carboxylic acid

HRID 1200129Notes

Reaction equation

HRID 1200129 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

  1. filtrationThe precipitates were collected by filtration
  2. dry with materialdried over phosphorus pentoxide

Sources & evidence

ORD record
ord-bf3d37d05af84a749f9e67d3febc6aca
Source dataset
uspto-grants-1990_02
Patent number
US04904652

Reaction notes

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