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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 509028생성일: 2026년 10월 26일

Pivaloyl chloride → N-(4-Chloro-5-(1-(4-chlorophenyl)-4,5-dihydro-5-oxo-1H-1,2,4-triazol-3-yl)-2-fluorobenzyl)pivalamide

https://huagongshe.com/reaction/509028

반응식

참여 물질

역할이름HCID투입량
반응물Pivaloyl chlorideHCID 62493—
반응물5-(5-(aminomethyl)-2-chloro-4-fluorophenyl)-2-(4-chlorophenyl)-2H-1,2,4-triazol-3 (4H)-oneHCID 136644848—
용매TetrahydrofuranHCID 8028—
생성물N-(4-Chloro-5-(1-(4-chlorophenyl)-4,5-dihydro-5-oxo-1H-1,2,4-triazol-3-yl)-2-fluorobenzyl)pivalamideHCID 136246046—

반응 단계

The title compound was prepared according to the procedure described in Example-108 by using 5-(5-(aminomethyl)-2-chloro-4-fluorophenyl)-2-(4-chlorophenyl)-2H-1,2,4-triazol-3(4H)-one (Intermediate-78, 0.120 g), pivaloyl chloride (0.5 mL), TEA (2.0 mL), dry THF (5 mL) to afford 0.033 g of the desired product. 1H NMR (300 MHz, DMSO): δ 1.12 (s, 9H), 4.30 (br s, 2H), 7.53-7.63 (m, 4H), 7.95 (d, J=12.8 Hz, 2H), 8.14 (s, 1H), 12.61 (s, 1H); MS (m/z): 437.47 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096545B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-edf5ce2e102b49c9bf07c84bec2ffda6
출처 메모uspto-grants-2015_08