Hydrochloric Acid → HCID 131712708, compound

HRID 434874Notes

Reaction equation

HRID 434874 reaction equation
[CH3:1][O:2][N:3]=[C:4]([C:31]1[N:32]=[C:33]([NH:36]C=O)[S:34][CH:35]=1)[C:5]([NH:7][CH:8]1[C:29](=[O:30])[N:10]2[C:11]([C:26]([OH:28])=[O:27])=[C:12]([CH2:15][O:16][C:17]([N:19]3[CH2:24][CH2:23][N:22]([CH3:25])[CH2:21][CH2:20]3)=[O:18])[CH2:13][S:14][C@H:9]12)=[O:6].FC(F)(F)C([O-])=O.[ClH:46]>CO>[ClH:46].[ClH:46].[CH3:1][O:2][N:3]=[C:4]([C:31]1[N:32]=[C:33]([NH2:36])[S:34][CH:35]=1)[C:5]([NH:7][CH:8]1[C:29](=[O:30])[N:10]2[C:11]([C:26]([OH:28])=[O:27])=[C:12]([CH2:15][O:16][C:17]([N:19]3[CH2:20][CH2:21][N:22]([CH3:25])[CH2:23][CH2:24]3)=[O:18])[CH2:13][S:14][C@H:9]12)=[O:6]

Participants

5

Procedure

To a solution of 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(4-methyl-1-piperazinyl)carbonyloxymethyl-3-cephem-4-carboxylic acid.trifluoroacetate (syn isomer) (1.0 g) in methanol (20 ml) was added conc.hydrochloric acid (0.62 ml) followed by stirring for 2 hours at ambient temperature. The reaction mixture was evaporated and the residue was pulverized in ethyl acetate, collected by filtration, washed with ethyl acetate and diethyl ether and then dried to give 7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(4-methyl-1-piperazinyl)carbonyloxymethyl-3-cephem-4-carboxylic acid.dihydrochloride (syn isomer).

Workup

  1. customThe reaction mixture was evaporated
  2. filtrationcollected by filtration
  3. washwashed with ethyl acetate and diethyl ether
  4. customdried

Sources & evidence

ORD record
ord-f9c92e942f6344448ad76cb75eaa1a77
Source dataset
uspto-grants-1983_08
Patent number
US04399278

Reaction notes

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