HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Methylamino-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylthiourea | HCID 2723704 | — |
| Reactant | 4-Bromo-3'-trifluoromethylacetoacetanilide | HCID 22347696 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methylamino-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole | HCID 21321158 | 81% |
Reaction Steps
A solution containing 32.4 g (0.10 mole) of 4-bromo-3'-trifluoromethylacetoacetanilide and 11.3 g (0.13 mole) of N-methylthiourea in 250 ml of ethanol was refluxed for four hours. The reaction mixture was poured into 700 ml of water and ethanol was added. A small quantity of insoluble material was removed by filtration and the filtrate was made strongly alkaline by the addition of ammonium hydroxide. The solution was cooled and an additional 400 ml of water was added. The precipitated solid was collected and dried in an oven. There was obtained 25.5 g (81%) of product, m.p. 153°-55°. N.M.R. (dimethyl-d6 sulfoxide) ∂ 2.8-2.9 (CH3, doublet), 3.5 (CH2), 6.3 (hetero-aromatic), 7.3-8.1 (aromatic, NH), 10.4 (HNC=0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152329 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-cab0f933c0154620b00895b6d501237f |
| Source note | uspto-grants-1979_05 |