Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915592생성일: 2026년 10월 26일
Lithium N-methylmethanaminide → 2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-(dimethylamino)benzoic acid
https://huagongshe.com/reaction/915592
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium N-methylmethanaminide | HCID 5152226 | — |
| 반응물 | 2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-fluorobenzoic acid | HCID 58958582 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-(dimethylamino)benzoic acid | HCID 58958609 | 15% |
반응 단계
To a solution of 2-{[3-tert-butyl-1-(2-methylphenyl)-1H-pyrazol-5-yl]amino}-4-fluorobenzoic acid (Example 248, 35 mg, 0.09 mmol) in THF (1 mL) at −40° C. was added LiNMe2 (0.19 mL, 1 M in hexanes) under nitrogen. The mixture was then stirred at this temperature for 30 min, and then gradually warmed to rt over a 4 h period. The pH of the solution was adjusted to pH 5, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude was purified by HPLC using gradient elution from 10 to 80% acetonitrile in water to afford 5.7 mg (15%) of the title compound. 1H NMR (300 MHz, CD2Cl2) δ 9.55 (s, 1H), 7.73 (d, 1H), 7.22-7.35 (m, 4H), 6.44 (d, 1H), 6.18 (dd, 1H), 6.15 (s, 1H), 3.00 (s, 6H), 2.04 (s, 3H), 1.32 (s, 9H). ES-MS m/z 393.2 (MH30 ); HPLC RT (min) 2.84.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07265144B2 |
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| 출처 데이터셋 | uspto-grants-2007_09 |
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| ORD ID | ord-8c2db87082454790adc8c54f20ad1b7c |
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| 출처 메모 | uspto-grants-2007_09 |
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