HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 13145506, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1,3,4-Thiadiazol-2-amine | HCID 19909 | — |
| Reactant | 2-(((Benzyloxy)carbonyl)amino)-4-methylpentanoic acid | HCID 246673 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13145506 | HCID 13145506 | 71.4% |
Reaction Steps
9.6 g of N-benzyloxycarbonyl-DL-leucine and 3.7 g of triethylamine were dissolved in 150 ml of chloroform, to which was added dropwise 3.9 g of ethyl chlorocarbonate under sodium chloride-ice cooling conditions. The solution was stirred for 2 hours, to which was then added 3.7 g of 2-amino-1,3,4-thiadiazole, followed by stirring for further 24 hours. The reaction solution was washed with water, and after drying, the solvent was removed by distillation to obtain 9.0 g (yield: 71%) of 2-(N-benzyloxycarbonyl-DL-leucylamino)-1,3,4-thiadiazole as white crystals having a melting point of 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382142 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-ecd81b84f7fc4cf99eeaf1635f861a37 |
| Source note | uspto-grants-1983_05 |