HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474367Generated: October 29, 2026
Diisopropylethylamine → 5-chloro-N-(1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide
https://huagongshe.com/reaction/474367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(3-Trifluoromethylphenyl)-2H-pyrazol-3-ylamine | HCID 43316770 | — |
| Reactant | 5-Chloropyrazolo[1,5-a]pyrimidine-3-carbonyl chloride | HCID 58063136 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-chloro-N-(1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide | HCID 58063110 | 58.7% |
Reaction Steps
To a stirred solution of 1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-amine (200 mg, 0.88 mmol) in dichloromethane (30 mL) was added 5-chloropyrazolo[1,5-a]pyrimidine-3-carbonyl chloride (215 mg, 1.0 mmol) and diisopropylethylamine (130 mg, 1.0 mmol). The mixture was heated to 50° C. overnight. After cooling to room temperature, the mixture was concentrated to afford crude 5-chloro-N-(1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide (210 mg, yield 58%), which was used for the next step without further purification. MS (ESI) m/z: 407.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637526B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-af9af61c59c34225bfe8c47e59d73f36 |
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| Source note | uspto-grants-2014_01 |
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