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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049174Generated: November 1, 2026

Formic Acid → 3-Acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-vinyloxyimino-acetamido]-ceph-3-eme-4-carboxylic acid

https://huagongshe.com/reaction/2049174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantSodium 3-acetoxymethyl-7-[2-(2-tritylamino-4-thiazolyl)-2-vinyloxyimino-acetamido]-ceph-3-eme-4-carboxylateHCID 131711732—
SolventWaterHCID 962—
Product3-Acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-vinyloxyimino-acetamido]-ceph-3-eme-4-carboxylic acidHCID 131711734—

Reaction Conditions

Temperature40 °C

Reaction Steps

1.612 g of the sodium salt of Example 35 was added to 4 ml of 98% formic acid and immediately after, 4 ml of distilled water were added thereto and the mixture was stirred for 15 minutes at 40° C. The heterogenous mixture was triturated for 30 minutes at room temperature and was vacuum filtered at 20° C. The filter was rinsed twice with 1.6 ml of 50% formic acid and the filtrate was evaporated to dryness. The residue was taken up in 5 ml of distilled w ater and the mixture was vacuum filtered at room temperature. The recovered product was rinsed with distilled water and then with ether and dried to obtain 300 mg of the syn isomer of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-vinyloxyimino-acetamido]-ceph-3-eme-4-carboxylic acid. Reextraction of insolubles with 50% formic acid recovered another 0.214 g of the said product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04196205
Source datasetuspto-grants-1980_04
ORD IDord-0abb8e21d1f3422d9ed5e2914a1bc6b4
Source noteuspto-grants-1980_04