Hydrochloric Acid → HCID 131713212, compound

HRID 1154253Notes

Reaction equation

HRID 1154253 reaction equation
[CH:1]1([O:6][N:7]=[C:8]([C:26]2[N:27]=[C:28]([NH:31]C=O)[S:29][CH:30]=2)[C:9]([NH:11][CH:12]2[C:24](=[O:25])[N:14]3[C:15]([C:21]([OH:23])=[O:22])=[C:16]([CH:19]=[CH2:20])[CH2:17][S:18][C@H:13]23)=[O:10])[CH2:5][CH2:4][CH:3]=[CH:2]1.Cl.O.C(=O)(O)[O-].[Na+]>CO.O1CCCC1.C(OCC)(=O)C>[CH:1]1([O:6][N:7]=[C:8]([C:26]2[N:27]=[C:28]([NH2:31])[S:29][CH:30]=2)[C:9]([NH:11][CH:12]2[C:24](=[O:25])[N:14]3[C:15]([C:21]([OH:23])=[O:22])=[C:16]([CH:19]=[CH2:20])[CH2:17][S:18][C@H:13]23)=[O:10])[CH2:5][CH2:4][CH:3]=[CH:2]1

Participants

8

Procedure

A mixture of 7-[2-(2-cyclopenten-1-yloxyimino)-2-(2-formamidothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (3.1 g) in methanol (22 ml), tetrahydrofuran (10 ml) and conc. hydrochloric acid (1.3 g) was stirred for 2.5 hours at ambient temperature. The reaction mixture was added to a mixture of water and ethyl acetate, and adjusted to pH 7.5 with a saturated aqueous sodium bicarbonate. The separated aqueous layer was adjusted to pH 3.0 with 10% hydrochloric acid. The precipitates were filtered off, washed with water and dried over phosphorus pentoxide in vacuo to give 7-[2-(2-cyclopenten-1-yloxyimino)-2-(2-aminothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (2.7 g).

Workup

  1. filtrationThe precipitates were filtered off
  2. washwashed with water
  3. dry with materialdried over phosphorus pentoxide in vacuo

Sources & evidence

ORD record
ord-91aa87aa6cb64e149631abdd8a074a82
Source dataset
uspto-grants-1984_12
Patent number
US04487927

Reaction notes

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