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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2287715생성일: 2026년 10월 26일

2-(Aminomethyl)aniline → 4-N-[(2-aminophenyl)methyl]pyrido[4,3-d]pyrimidine-4,7-diamine

https://huagongshe.com/reaction/2287715

반응식

참여 물질

역할이름HCID투입량
반응물2-(Aminomethyl)anilineHCID 178096—
반응물7-Amino-4-methylthiopyrido[4,3-d]pyrimidineHCID 10442562—
용매IsopropanolHCID 3776—
생성물4-N-[(2-aminophenyl)methyl]pyrido[4,3-d]pyrimidine-4,7-diamineHCID 532809047.1%

반응 단계

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (136 mg, 0.71 mmol) (described in a previous experimental) and 2-aminobenzylamine (1.70 g, 13.8 mmol) in isopropanol (5 mL) is stirred at reflux for 1 h, and the resulting product is chromatographed on silica gel (7-20% EtOH/EtOAc) and alumina (6-10% EtOH/CHCl3) to give 7-amino-4-(2-aminobenzylamino)pyrido[4,3-d]pyrimidine (89 mg, 47%) as a white solid. 1H NMR (DMSO) δ 9.08 (1H, s), 8.68 (1H, t, J=5.8 Hz), 8.26 (1H, s), 7.05 (1H, d, J=7.4 Hz), 6.96 (1H, t, J=7.6 Hz), 6.63 (1H, d, J=7.9 Hz), 6.51 (1H, t, J=7.4 Hz), 6.46 (2H, brs), 6.35 (1H, s), 5.20 (2H, brs), 4.56 (2H, d, J=5.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06084095
출처 데이터셋uspto-grants-2000_07
ORD IDord-acdb23c36e67429fb8e55818f6b163af
출처 메모uspto-grants-2000_07