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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2287705생성일: 2026년 10월 25일

2-(Trifluoromethyl)aniline → 4-N-[2-(trifluoromethyl)phenyl]pyrido[4,3-d]pyrimidine-4,7-diamine

https://huagongshe.com/reaction/2287705

반응식

참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)anilineHCID 6922—
반응물Sodium BicarbonateHCID 516892—
반응물7-Amino-4-methylthiopyrido[4,3-d]pyrimidineHCID 10442562—
반응물Alpha,alpha,alpha-trifluoro-O-toluidine hydrochlorideHCID 22736790—
용매Chloroform methanolHCID 21584188—
생성물4-N-[2-(trifluoromethyl)phenyl]pyrido[4,3-d]pyrimidine-4,7-diamineHCID 532805741%

반응 조건

온도160 °C

반응 단계

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (300 mg, 1.56 mmol), 2-aminobenzotrifluoride hydrochloride (1.00 g, 5.06 mmol) and 2-aminobenzotrifluoride (2.00 g, 12.4 mmol) is stirred at 160° C. for 10 min. The resulting product is neutralized with excess NaHCO3, dissolved in MeOH/CHCl3, dried onto silica gel and chromatographed over silica gel (6-7% MeOH/CH2Cl2) to give 7-amino-4-(2-trifluoromethylanilino)pyrido[4,3-d]pyrimidine (194 mg, 41%) as a cream solid, mp (MeOH/CHCl3 /light petroleum) 126-130° C. (dec.). 1H NMR (DMSO) δ 10.60 (1H, brs), 9.17 (1H, brs), 8.13 (1H, brs), 7.76, 7.69 (1H, 1H, m, m), 7.45 (2H, m), 6.66 (2H, brs), 6.36 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06084095
출처 데이터셋uspto-grants-2000_07
ORD IDord-9fb8c8cb8f79493599435b58936c2691
출처 메모uspto-grants-2000_07