Hydrochloric Acid → 7-[2-(2-cyclopenten-1-yl)oxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-[1-(2-carboxy-2-hydroxyiminoethyl)-1H-tetrazole-5-yl]thiomethyl-3-cephem-4-carboxylic acid

HRID 904876Notes

Reaction equation

HRID 904876 reaction equation
[CH:1]1([O:6][N:7]=[C:8]([C:38]2[N:39]=[C:40]([NH:43]C=O)[S:41][CH:42]=2)[C:9]([NH:11][CH:12]2[C:36](=[O:37])[N:14]3[C:15]([C:33]([OH:35])=[O:34])=[C:16]([CH2:19][S:20][C:21]4[N:25]([CH2:26][C:27]([C:30]([OH:32])=[O:31])=[N:28][OH:29])[N:24]=[N:23][N:22]=4)[CH2:17][S:18][C@H:13]23)=[O:10])[CH2:5][CH2:4][CH:3]=[CH:2]1.Cl>CO.O1CCCC1>[CH:1]1([O:6][N:7]=[C:8]([C:38]2[N:39]=[C:40]([NH2:43])[S:41][CH:42]=2)[C:9]([NH:11][CH:12]2[C:36](=[O:37])[N:14]3[C:15]([C:33]([OH:35])=[O:34])=[C:16]([CH2:19][S:20][C:21]4[N:25]([CH2:26][C:27]([C:30]([OH:32])=[O:31])=[N:28][OH:29])[N:24]=[N:23][N:22]=4)[CH2:17][S:18][C@H:13]23)=[O:10])[CH2:5][CH2:4][CH:3]=[CH:2]1

Participants

5

Procedure

A solution of 7-[2-(2-cyclopenten-1-yl)oxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-[1-(2-carboxy-2-hydroxyiminoethyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylic acid (syn isomer: in the 7-position) (1.1 g) and conc. hydrochloric acid (0.12 g) in methanol (10 ml) and tetrahydrofuran (2 ml) was stirred at room temperature for 2.5 hours. After removal of organic solvents under reduced pressure, the residue was dissolved in an aqueous solution of sodium bicarbonate and the solution was adjusted to pH 7.5. The aqueous solution was washed with ethyl acetate (15 ml) and then adjusted to pH 3.0 with 10% hydrochloric acid to give precipitates which were filtered and washed with water to give 7-[2-(2-cyclopenten-1-yl)oxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-[1-(2-carboxy-2-hydroxyiminoethyl)-1H-tetrazole-5-yl]thiomethyl-3-cephem-4-carboxylic acid (syn isomer: in the 7-position).

Workup

  1. customAfter removal of organic solvents under reduced pressure
  2. dissolutionthe residue was dissolved in an aqueous solution of sodium bicarbonate
  3. washThe aqueous solution was washed with ethyl acetate (15 ml)
  4. customto give
  5. customprecipitates which
  6. filtrationwere filtered
  7. washwashed with water

Sources & evidence

ORD record
ord-8d527991264c4a8dbdebebab0bbb5274
Source dataset
uspto-grants-1983_12
Patent number
US04420477

Reaction notes

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