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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59542생성일: 2026년 10월 23일

3,3-Dimethyl-1-butyne → N-(4-Chloro-2-fluoro-5-(4,5-dihydro-3-(4-(3,3-dimethylbut-1-ynyl)phenyl)-5-oxo-1,2,4-triazol-1-yl)benzyl)pivalamide

https://huagongshe.com/ko/reaction/59542

반응식

참여 물질

역할이름HCID투입량
반응물3,3-Dimethyl-1-butyneHCID 13512—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물N-(4-chloro-2-fluoro-5-(4,5-dihydro-3-(4-iodophenyl)-5-oxo-1,2,4-triazol-1-yl)benzyl)pivalamideHCID 136492379—
촉매HCID 178418476HCID 178418476—
용매Dimethyl SulfoxideHCID 679—
생성물N-(4-Chloro-2-fluoro-5-(4,5-dihydro-3-(4-(3,3-dimethylbut-1-ynyl)phenyl)-5-oxo-1,2,4-triazol-1-yl)benzyl)pivalamideHCID 13624607754.8%

반응 단계

The title compound was prepared according to the procedure described in Example-111 using N-(4-chloro-2-fluoro-5-(4,5-dihydro-3-(4-iodophenyl)-5-oxo-1,2,4-triazol-1-yl)benzyl)pivalamide (Intermediate-90, 0.100 g, 0.189 mmol), 3,3-dimethylbut-1-yne (0.031 g, 0.378 mmol), TBAF (0.178 g, 0.567 mmol), bis(triphenylphosphine)palladium(II) chloride (catalytic) and DMSO (3.0 mL) to afford 0.050 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 1.10 (s, 9H), 1.30 (s, 9H), 4.30 (d, J=9.0 Hz, 2H), 7.43-7.50 (m, 3H), 7.65 (d, J=9.3 Hz, 1H), 7.78 (d, J=8.1 Hz, 2H), 8.14 (br s, 1H), 12.60 (br s, 1H); MS (m/z): 483.29 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09439890B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d33e135dac6d487eba81cb52dad25574
출처 메모uspto-grants-2016_09