참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dibutylamine | HCID 8148 | — |
| 반응물 | Potassium Sodium Tartrate | HCID 9357 | — |
| 반응물 | ethyl 4-chloro-5-methyl-1H-pyrazole-3-carboxylate | HCID 604759 | — |
| 반응물 | Trimethylaluminum | HCID 16682925 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N,N-dibutyl-4-chloro-5-methyl-1H-pyrazole-3-carboxamide | HCID 71062189 | 69.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09126980B2 |
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| 출처 데이터셋 | uspto-grants-2015_09 |
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| ORD ID | ord-7ff561779ea549daa6e5b98eaae88a0e |
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| 출처 메모 | uspto-grants-2015_09 |
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