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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1948744생성일: 2026년 10월 25일

2-Amino-4-chloro-6-methylpyrimidine → N4,6-Dimethyl-N4-[(8-methyl-2-phenylquinolin-3-yl)methyl]pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1948744

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-chloro-6-methylpyrimidineHCID 21810—
반응물DiisopropylethylamineHCID 81531—
반응물8-Methyl-2-phenylquinoline-3-carboxaldehydeHCID 833680—
반응물TriacetoxyborohydrideHCID 2724942—
반응물Methylamine hydrochlorideHCID 6364545—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N4,6-Dimethyl-N4-[(8-methyl-2-phenylquinolin-3-yl)methyl]pyrimidine-2,4-diamineHCID 8665303420.3%

반응 단계

A mixture of 8-methyl-2-phenylquinoline-3-carboxaldehyde (100 mg, 0.4 mmol), methylamine hydrochloride (120 mg, 1.8 mmol) and DIPEA (230 mg, 1.8 mmol) in DCM (20 mL) was treated with titanium(IV) n-propoxide (228 mg, 0.8 mmol). The reaction mixture was stirred at r.t. for 18 h. The solvent was removed in vacuo and the residue dissolved in THF (20 mL) before triacetoxyborohydride (170 mg, 0.8 mmol) was added. The reaction mixture was stirred at r.t. for 2 h, the solvent removed in vacuo and the residue partitioned between DCM (100 mL) and water (30 mL). The organic layer was separated, dried (MgSO4) and the solvent removed in vacuo. The residue was dissolved in NMP (2 mL) and to this solution was added DIPEA (230 mg, 1.8 mmol) and 2-amino-4-chloro-6-methylpyrimidine (57 mg, 0.4 mmol). The mixture was heated in a microwave at 220° C. for 2 h. Purification by preparative HPLC (Method 1) gave the title compound as an off-white solid (30 mg, 20%). δH (CDCl3) 7.82 (s, 1H), 7.62-7.70 (m, 2H), 7.61 (d, J 7.9 Hz, 1H), 7.46-7.55 (m, 5H), 5.75 (s, 1H), 4.93 (s, 2H), 4.67 (s, 2H), 2.93 (s, 3H), 2.82 (s, 3H), 2.22 (s, 3H). LCMS (ES+) 370.2 (M+H)+, RT 2.36 minutes (Method 3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399483B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-99bafe0f00184fe1b4e7347d3607d504
출처 메모uspto-grants-2013_03