HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(1,1-dimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,1-Dimethyl-2,3-dihydro-1H-inden-4-amine | HCID 13115615 | — |
| Reactant | 2-Chloro-4-methylthiazole-5-carboxylic acid chloride | HCID 13593393 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1,1-dimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide | HCID 14535761 | 93% |
Reaction Steps
To a solution of 0.82 g (5.07 mmol) of 1,1-dimethyl-4-aminoindan and 0.48 g (6.08 mmol) of pyridine in 10 ml of tetrahydrofuran was added dropwise with stirring below 5° C. under ice cooling, a solution of 0.99 g (5.07 mmol) of 2-chloro-4-methylthiazole-5-carboxylic acid chloride in 3 ml of tetrahydrofuran, followed by stirring at room temperature overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with 5% hydrochloric acid and then water and was dried over anhydrous sodium sulfate. The solvent was distilled off to obtain crystals, which was washed with n-hexane and dried to obtain 1.51 g of N-(1,1-dimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide (yeild 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837242 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-cbb78989544144cab9e54c73d9219a5f |
| Source note | uspto-grants-1989_06 |