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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11882생성일: 2026년 10월 25일

Benzylamine → N-benzyl-5-(3,4-dichlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxamide

https://huagongshe.com/reaction/11882

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물TriethylamineHCID 8471—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물5-(3,4-Dichlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acidHCID 1083675—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물N-benzyl-5-(3,4-dichlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxamideHCID 111131989.9%

반응 단계

Benzotriazol-1-yloxy-tris(dimethylamino)-phosphonium hexafluorophosphate (BOP) (0.845 g, 1.91 mmol) was added to a suspension of 5-(3,4-dichloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid (0.600 g, 1.59 mmol) and benzylamine (0.209 mL, 1.91 mmol) in tetrahydrofuran (25 ml) containing triethylamine (0.665 mL, 4.77 mmol). The reaction mixture was stirred overnight at room temperature, diluted with ethyl ether (25 mL) and washed with a saturated aqueous solution of sodium bicarbonate (50 mL). The organic layer was collected, concentrated under reduced pressure and the crude product was purified by column chromatography on silica gel to give 5-(3,4-dichloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid benzylamide (0.665 g, 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098335B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ad52a17fa51e4b88856111c6d4ba70a8
출처 메모uspto-grants-2006_08