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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127099Generated: November 2, 2026

Hydrochloric Acid → HCID 131712110, compound

https://huagongshe.com/reaction/127099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantAgr 307HCID 73233—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20130112HCID 20130112—
ReactantHCID 70572016HCID 70572016—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 131712110HCID 131712110—

Reaction Steps

A mixture of 2-(2-aminothiazol-4-ylmethyl)isothiourea (1.57 g.) and 1 N sodium hydroxide (24 ml.) was stirred for 15 minutes at room temperature, and then the mixture was adjusted to pH 9 with 1 N hydrochloric acid (12 ml.). Thus obtained solution containing 2-aminothiazol-4-ylmethanethiol was dropwise added to a mixture of 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-bromoacetamido-3-cephem-4-carboxylic acid (2.16 g.), sodium bicarbonate (0.67 g.), water (33 ml.) and ethanol (33 ml.) over 15 minutes at room temperature with stirring. The mixture was stirred for 1 hour at room temperature, and it was adjusted to pH 4 with 1 N hydrochloric acid. The mixture was allowed to stand for overnight in a refrigerator, and the precipitates were collected by filtration, washed with a small amount of water and then dried to give powder of 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-(2-aminothiazol-4-yl)methylthioacetamido-3-cephem-4-carboxylic acid (0.7 g.), mp 180° to 250° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254260
Source datasetuspto-grants-1981_03
ORD IDord-74f9edd6201f4b688b517b008f72ced3
Source noteuspto-grants-1981_03