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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443533Generated: October 29, 2026

Sodium Bicarbonate → HCID 131710311, compound

https://huagongshe.com/reaction/443533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantα-(Chlorocarbonyl)benzenemethanesulfonic acidHCID 13127332—
ReactantHCID 23620956HCID 23620956—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 131710311HCID 131710311—

Reaction Steps

The α-sulfo-acylamido-3-halo-cephem compounds of the Formula I wherein Q is a sulfo group (-SO3H) are prepared by following the acylation procedures employed for the preparation of α-sulfobenzylpenicillins described by U.S. Pat. No. 3,660,379 and in the J. Med. Chem., 15 (11), 11-5 (1972); ibid, p. 1108. For example, 7-amino-3-chloro-3-cephem-4-carboxylic acid is reacted with α-sulfophenylacetyl chloride in a mixture of acetone and water containing an excess of sodium bicarbonate to yield 7-(α-sulfophenylacetamido)-3-chloro-3-cephem-4-carboxylic acid. Examples of α-sulfoacylamido-3-halo-cephems of the present invention are,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260745
Source datasetuspto-grants-1981_04
ORD IDord-06426f0cc2f541cf9f5aae277ada8b48
Source noteuspto-grants-1981_04