HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(N-isobutyryl-N-methylamino)-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 2-Methylamino-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole | HCID 21321158 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(N-isobutyryl-N-methylamino)-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole | HCID 21321161 | 60.2% |
Reaction Steps
A solution containing 7.6 g (0.025 mole) of 2-methylamino-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole and 2.9 g (0.027 mole) of isobutyryl chloride in 25 ml of pyridine was heated at about 45° for 24 hours. The mixture was poured into water. The thick oil failed to crystallize. The aqueous phase was decanted and the residue was dissolved in benzene. The organic phase was washed with water, dried over sodium sulfate and cooled. With stirring, hexane was added and a crystalline product precipitated. There was obtained 5.8 g of the desired amide, m.p. 122°-23°. N.M.R. (dimethyl-d6 sulfoxide) ∂ 1.1-1.3 (2×CH3), 2.7-3.4 (CH, septet), 3.6 (NCH3), 3.7 (CH2), 6.9 (hetero-aromatic), 7.3-8.1 (aromatic), 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-08ed975b7d2942a6b4c533e751db8bae |
| Source note | uspto-grants-1979_05 |