HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252164Generated: October 25, 2026
Water → 5-chloro-1-methyl-3-trifluoromethyl-N-(1,1-dimethylindane-4-yl)pyrazole-4-carboxamide
https://huagongshe.com/reaction/1252164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride | HCID 2794585 | — |
| Reactant | 1,1-Dimethyl-2,3-dihydro-1H-inden-4-amine | HCID 13115615 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-chloro-1-methyl-3-trifluoromethyl-N-(1,1-dimethylindane-4-yl)pyrazole-4-carboxamide | HCID 13920721 | 81.1% |
Reaction Steps
To a solution of 1.61 g of 1,1-dimethyl-4-aminoindane and 2 ml of pyridine in 50 ml of toluene was added drop by drop with stirring at room temperature a solution of 2.47 g of 5-chloro-1-methyl-3-trifluoromethylpyrazole-4-carboxylic acid chloride in 10 ml of toluene, followed by stirring at room temperature for 12 hours. Thereafter, the reaction solution was poured into a cold water to result in separation into two layers. The aqueous layer was extracted with ethyl acetate. The resultant organic layer was dried over anhydrous magnesium sulfate and the soluent was distilled off. The residue was recrystallized using toluene to obtain 3.01 g of 5-chloro-1-methyl-3-trifluoromethyl-N-(1,1-dimethylindane-4-yl)pyrazole-4-carboxamide having a melting point of 119.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742074 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-a8d03a69425d4a02b93aee7f9c20ed2b |
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| Source note | uspto-grants-1988_05 |
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