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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 558899생성일: 2026년 10월 26일

Trifluoroacetic acid → 5-[7-Trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-thiophene-2-sulfonic acid pyridin-3-ylamide

https://huagongshe.com/reaction/558899

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물5-bromo-N-(pyridin-3-yl)thiophene-2-sulfonamideHCID 933073—
반응물3-Ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 71539732—
용매DichloromethaneHCID 6344—
생성물5-[7-Trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-thiophene-2-sulfonic acid pyridin-3-ylamideHCID 86608120—

반응 단계

The title compound was prepared from 3-ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (example C.1) (178 mg, 0.5 mmol) and commercially available 5-bromo-thiophene-2-sulfonic acid pyridin-3-ylamide [CAS-No. 439934-18-6] (160 mg, 0.5 mmol) according to general procedure II and subsequent cleavage of the protecting group with TFA in dichloromethane at 0° C. Obtained as a yellow solid (200 mg, 67%). MS (ISN) 592.1 [(M−H)−]; mp 248° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063048B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-f1eb446409624dd1b1ef6722aa4fe516
출처 메모uspto-grants-2011_11