HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245606Generated: October 30, 2026
Isopropylamine → 6-{[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl]-amino}-1H-indole-7-carboxylic acid isopropylamide
https://huagongshe.com/reaction/245606
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 7-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-1H-8-oxa-1,6-diaza-cyclopenta[a]naphthalen-9-one | HCID 136176026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-{[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl]-amino}-1H-indole-7-carboxylic acid isopropylamide | HCID 57990166 | 16% |
Reaction Steps
To a solution of 110 mg (0.25 mmol) of the crude 7-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-1H-8-oxa-1,6-diaza-cyclopenta[a]naphthalen-9-one in 2.5 mL of anhydrous tetrahydrofuran, under Argon, is added 0.07 mL (0.77 mmol) of isopropylamine. The reaction is stirred during 5 hours at ambient temperature and then quenched with an aqueous saturated solution of ammonium chloride. The product is extracted twice with ethyl acetate and the combined organic phases are dried on Na2SO4, filtrated and the solvent is evaporated. After purification by flash chromatography on silica gel with hexanes and ethyl acetate as eluents and a preparative thin layer chromatography, 18.5 mg (0.04 mmol, 16%) of a white solid are obtained; LC/MS:513/515 (M+Na)+, m.p.: 240-242° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658801B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-2042812cf56f46dab18f4e8b1865964b |
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| Source note | uspto-grants-2014_02 |
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