Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240747생성일: 2026년 10월 25일
Diisopropylethylamine → 5-Cyclopropyl-6-cyclopropylmethoxy-nicotinic acid N'-(4-fluoro-phenyl)-N'-methyl-hydrazide
https://huagongshe.com/reaction/240747
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 반응물 | 5-Cyclopropyl-6-cyclopropylmethoxy-nicotinic acid | HCID 71293986 | — |
| 반응물 | 1-(4-Fluorophenyl)-1-methylhydrazine hydrochloride | HCID 86678105 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Cyclopropyl-6-cyclopropylmethoxy-nicotinic acid N'-(4-fluoro-phenyl)-N'-methyl-hydrazide | HCID 71294311 | 97.5% |
반응 단계
In a 10 mL two-necked flask, the above prepared 5-cyclopropyl-6-cyclopropylmethoxy-nicotinic acid (70 mg, 300 μmol, Eq: 1.00) was combined with tetrahydrofuran (3 mL) and DMF (1 mL) to give a colorless solution. TBTU (145 mg, 450 μmol, Eq: 1.5) and N,N-diisopropylethylamine (194 mg, 262 μl, 1.5 mmol, Eq: 5) were added and the reaction mixture stirred for 10 min at rt, before 1-(4-fluorophenyl)-1-methylhydrazine hydrochloride (63.6 mg, 360 μmol, Eq: 1.2, CAN 1978-54-7) was added and the reaction mixture kept overnight at rt. The reaction mixture was quenched with 1 M HCl (10 mL) and extracted with EtOAc (2×20 mL). The organic layers were washed with 1 M NaOH, then with H2O/NaCl solution, combined, dried over Na2SO4 and concentrated in vacuo. The crude material was eventually purified by flash chromatography (silica gel, 20 g, 15% to 40% EtOAc in heptane) to provide 104 mg of the title product as colorless oil; MS (EI) 354.6 (M−H)−.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08648099B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-5c16ff33277747f4b8094a70b40f75ea |
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| 출처 메모 | uspto-grants-2014_02 |
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