HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(1,1,3-trimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloro-4-methyl-1,3-thiazole-5-carboxylic acid | HCID 666960 | — |
| Reactant | 1,1,3-Trimethylindan-4-amine | HCID 11217541 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1,1,3-trimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide | HCID 14535768 | 43% |
Reaction Steps
252 mg (1.42 mmol) of 2-chloro-4-methylthiazole-5-carboxylic acid and 442 mg (1.42 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimidomethiodide were dissolved in 10 ml of methylene chloride and stirred at room temperature for 1 hour. Then, to the solution was added 249 mg (1.42 mmol) of 1,1,3-trimethyl-4-aminoindan and reaction was effected for 6 hours under reflux. The reaction mixture was poured into water and extracted with methylene chloride. The organic layer was concentrated and thereafter was purified by column chromatography (eluent; n-hexane:ethyl acetate=50:50 V/V) to obtain 204 mg of N-(1,1,3-trimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide (yield 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837242 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-935a7dab9601420ab3629bc3d7fc8dce |
| Source note | uspto-grants-1989_06 |