돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물Lithium N-methylmethanaminideHCID 5152226—
반응물2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-fluorobenzoic acidHCID 58958582—
용매TetrahydrofuranHCID 8028—
생성물2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-(dimethylamino)benzoic acidHCID 5895860915%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265144B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-8c2db87082454790adc8c54f20ad1b7c
출처 메모uspto-grants-2007_09