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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2274577생성일: 2026년 10월 26일

Dibutylamine → N,N-dibutyl-4-chloro-5-methyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/2274577

반응식

참여 물질

역할이름HCID투입량
반응물DibutylamineHCID 8148—
반응물Potassium Sodium TartrateHCID 9357—
반응물ethyl 4-chloro-5-methyl-1H-pyrazole-3-carboxylateHCID 604759—
반응물TrimethylaluminumHCID 16682925—
용매DichloromethaneHCID 6344—
생성물N,N-dibutyl-4-chloro-5-methyl-1H-pyrazole-3-carboxamideHCID 7106218969.2%

반응 단계

To a stirred solution of dibutylamine (13 mL, 76 mmol) in dichloromethane (250 mL) under nitrogen atmosphere was added trimethylaluminium (38 mL, 2M in toluene, 76 mmol). The mixture was stirred at ambient temperature for 30 minutes. (4-Chloro-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester (4.8 g, 25 mmol) in dichloromethane (30 mL) was added dropwise to the mixture. The reaction was stirred for 12 hours under a nitrogen atmosphere. The mixture was poured into saturated Rochelle salt solution slowly and stirred at ambient temperature for 2 hours. The organic layer was collected. The aqueous layer was extracted with dichloromethane and combined with the organic layer. The organic phase was brine-washed, dried over sodium sulfate, filtered, concentrated down, and dried. The residue was purified by eluting through a silica gel column with a 0 to 100% ethyl acetate/heptane gradient to afford the title compound (4.7 g, 68% yield) as a clear oil. MS (ESI) [m/e, (M+H)+]=272.4. 1H NMR (400 MHz, chloroform-d) δ ppm 3.50 (t, J=7.5 Hz, 2H), 3.37 (t, J=7.5 Hz, 2H), 2.28 (s, 3H), 1.64 (quin, J=7.5 Hz, 2H), 1.44-1.55 (m, 2H), 1.30-1.43 (m, 2H), 1.10-1.22 (m, 2H), 0.97 (t, J=8.0 Hz, 3H), 0.82 (t, J=7.3 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09126980B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-7ff561779ea549daa6e5b98eaae88a0e
출처 메모uspto-grants-2015_09