Ethyl Acetate → 7-(2-Methoxyimino-3-oxo-bromobutyramido)-3-cephem-4-carboxylic acid

HRID 1154812Notes

Reaction equation

HRID 1154812 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[CH3:5][O:6][N:7]=[C:8]([C:24](=[O:26])[CH3:25])[C:9]([NH:11][CH:12]1[C:22](=[O:23])[N:14]2[C:15]([C:19]([OH:21])=[O:20])=[CH:16][CH2:17][S:18][C@H:13]12)=[O:10].[BrH:27].[NH+]1C=CC=CC=1.C(OCC)(=O)C>O1CCCC1.O>[CH3:5][O:6][N:7]=[C:8]([C:24](=[O:26])[CH2:25][Br:27])[C:9]([NH:11][CH:12]1[C:22](=[O:23])[N:14]2[C:15]([C:19]([OH:21])=[O:20])=[CH:16][CH2:17][S:18][C@H:13]12)=[O:10]

Participants

7

Procedure

Aluminum chloride (120 mg.) was added to a solution of 7-(2-methoxyimino-3-oxobutyramido)-3-cephem-4-carboxylic acid (syn isomer, 50 mg.) in dry tetrahydrofuran (10 ml.). Pridinium hydrobromide perbromide (50 mg.) was added to the solution, and stirred at room temperature for 20 minutes. Ethyl acetate (50 ml.) and water (10 ml.) were added to the resultant solution and the mixture was treated in a similar manner to that of the above Example 10-(8) to give 7-(2-methoxyimino-3-oxo-4-bromobutyramido)-3-cephem-4-carboxylic acid (syn isomer, 52.5 mg.)

Workup

  1. additionthe mixture was treated in a similar manner to that of the above Example 10-(8)

Sources & evidence

ORD record
ord-e63ce43b861646d88d344e776bd2ee08
Source dataset
uspto-grants-1981_11
Patent number
US04298529

Reaction notes

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