HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → 2-amino-4-[N-4-chlorophenyl-N-methyl(carbamoylmethyl)] thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-bromo-4'-chloro-N-methylacetoacetanilide | HCID 20297528 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-amino-4-[N-4-chlorophenyl-N-methyl(carbamoylmethyl)] thiazole | HCID 54484717 | 66.7% |
Reaction Steps
A 500 ml reaction flask equipped with a condenser, magnetic stirrer, thermometer and heating mantle was charged with 20.2 g (0.066 mole) of 4-bromo-4'-chloro-N-methylacetoacetanilide, 200 ml of ethanol and 5.4 g (0.071 mole) of thiourea. The reaction solution was refluxed for three hours. After cooling, about one-half of the solvent was removed on the rotary evaporator and the solution was poured into 300 ml of water. After adding sufficient ammonium hydroxide to pH 8, additional water was added. The precipitated crystalline product was dried in a vacuum oven. There was obtained 12.4 g (66.7%) of white material, M.P. 148°-50°. N.M.R. (dimethyl-d6 sulfoxide, CDCl3) ∂3.2 (NCH3), 3.3 (CH2), 6.0 (heteroaromatic), 7.3-7.5 (aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232163 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-445ca06c839241da95e1f6d382f94a2a |
| Source note | uspto-grants-1980_11 |