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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858529Generated: November 1, 2026

Hydrochloric Acid → HCID 178433976, compound

https://huagongshe.com/reaction/1858529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178433975HCID 178433975—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178433976HCID 17843397652.3%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a suspension of 7β-[2-(5-chloro-2-formylaminothiazol-4-yl)acetamido]-3-(5-methyl-1,3,4-thiadiazol-2-yl)thio-3-cephem-4-carboxylic acid (380 mg), methanol (4 ml) and tetrahydrofuran (4 ml) was conc-hydrochloric acid (153 μl). The mixture was stirred for 5 hours at 35° C. The reaction mixture was added to a mixture of ethyl acetate (20 ml) and ice-water (50 ml). To the aqueous solution was added ethyl acetate (20 ml). The mixture was adjusted to pH 7 with 1N-sodium hydroxide solution. To the separated aqueous solution was added ethyl acetate (20 ml). The mixture was adjusted to pH 2 with 1N-hydrochloric acid. The precipitate was collected by filtration, washed with ethyl acetate, and dried to give 7β-[2-(2-amino-5-chlorothiazol-4-yl)acetamido]-3-(5-methyl-1,3,4-thiadiazol-2-yl)thio-3-cephem-4-carboxylic acid (188 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150351
Source datasetuspto-grants-2000_11
ORD IDord-e8bb8fb24c04427992b6568c8e5e3330
Source noteuspto-grants-2000_11