HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(5-Tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-methylaminothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methylthiourea | HCID 2723704 | — |
| Reactant | N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-4-bromoacetoacetamide | HCID 21321151 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(5-Tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-methylaminothiazole | HCID 21321159 | 87.2% |
Reaction Steps
A reaction mixture containing 11.4 g (0.035 mole) of N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-4-bromoacetoacetamide, 150 ml of ethanol and 3.3 g (0.036 mole) of N-methylthiourea was refluxed for four hours. The reaction solution was poured into 300 ml of water and treated with excess aqueous sodium bicarbonate. The product was isolated and dried. There was obtained 9.5 g (87.2%) of white solid, m.p. 198°-200° (dec.). N.M.R. (CDCl3) ∂ 1.4 [C(CH3)3 ], 3.0 (CH3), 3.8 (CH2), 6.4 (hetero-aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152329 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-d582eac5f7a14c52b888cef17df73c51 |
| Source note | uspto-grants-1979_05 |