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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178453124 | HCID 178453124 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 7-Amino-3-(5-t-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid | HCID 14207412 | 56.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04205166 |
|---|
| Source dataset | uspto-grants-1980_05 |
|---|
| ORD ID | ord-8acee22d982e4cbc8362d5145309fa0b |
|---|
| Source note | uspto-grants-1980_05 |
|---|