Acetic Acid → HCID 178475886, compound

HRID 444546Notes

Reaction equation

HRID 444546 reaction equation
Cl.[NH:2]=[C:3]1[NH:7][C:6]([C:8](=[N:29][OH:30])[C:9]([NH:11][CH:12]2[C:27](=[O:28])[N:14]3[C:15]([C:24]([OH:26])=[O:25])=[C:16]([CH2:19][O:20][C:21](=[O:23])[CH3:22])[CH2:17][S:18][C@H:13]23)=[O:10])=[CH:5][S:4]1.C(O)(=O)C.Cl.O>C(O)C>[NH:2]=[C:3]1[NH:7][C:6]([C:8](=[N:29][OH:30])[C:9]([NH:11][CH:12]2[C:27](=[O:28])[N:14]3[C:15]([C:24]([OH:26])=[O:25])=[C:16]([CH2:19][O:20][C:21](=[O:23])[CH3:22])[CH2:17][S:18][C@H:13]23)=[O:10])=[CH:5][S:4]1

Participants

6

Procedure

To a mixture of 0.309 g of 7-[2-(2-imino-4-thiazolin-4-yl)-2-hydroxyimino-acetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid hydrochloride (syn-isomer) and 1 ml of acetic acid there was added a sufficient amount of 1N-hydrochloric acid to completely dissolve the former. This solution was subjected to column chromatography on polystyrene resin (Amberlite XAD-2, Rohm & Haas Co.), development being carried out with water and 20% ethanol in the order mentioned. The fractions containing the desired product were pooled, concentrated and lyophilized. By the above procedure the captioned compound was obtained.

Workup

  1. dissolutionto completely dissolve the former

Sources & evidence

ORD record
ord-fcb17875cee645ee8649d0eb3caa3a85
Source dataset
uspto-grants-1981_04
Patent number
US04264595

Reaction notes

Loading…