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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395772Generated: October 27, 2026

Hydrochloric Acid → 7-Amino-3-(5-t-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1395772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178453124HCID 178453124—
SolventAcetoneHCID 180—
Product7-Amino-3-(5-t-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acidHCID 1420741256.2%

Reaction Steps

5-Tert-butoxycarbonylaminomethyl-1,3,4-thiadiazole-2-thiol (1.24 g.) was dissolved in acetone (10 ml.). The solution was added to the aqueous solution (40 ml.) containing sodium bicarbonate (0.84 g.). The mixed solution was warmed on water bath heating at 70°-75° C. To the solution was added all at once 7-aminocephalosporanic acid (1.35 g.) at 55° C. The mixture was stirred at 65°-70° C. for 2 hrs. and then cooled to 0°-5° C. with ice. The reaction mixture was adjusted to pH 5.0-5.2 with 10% hydrochloric acid. The precipitating pale yellow substance was separated out by filtration, washed with water and acetone, and then dried to give 7-amino-3-(5-tert-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid (1.28 g.). m.p. over than 220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04205166
Source datasetuspto-grants-1980_05
ORD IDord-8acee22d982e4cbc8362d5145309fa0b
Source noteuspto-grants-1980_05