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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491200생성일: 2026년 10월 25일

2-Chloro-5-methylpyrimidin-4-amine → 5-Methyl-N2-(4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/491200

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-5-methylpyrimidin-4-amineHCID 4302175—
반응물4-(2-(Pyrrolidin-1-yl)ethoxy)anilineHCID 6493749—
용매Acetic AcidHCID 176—
생성물5-Methyl-N2-(4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)pyrimidine-2,4-diamineHCID 5767508573%

반응 단계

A mixture of 2-chloro-5-methyl-pyrimidin-4-ylamine (0.50 g, 3.5 mmol) and 4-(2-pyrrolidin-1-yl-ethoxy)-phenylamine (1.1 g, 5.3 mmol) in acetic acid (8 mL) was sealed in a microwave reaction tube and irradiated with microwave at 150° C. for 15 min. After cooling to room temperature, the cap was removed and the mixture concentrated. The residue was taken in water (30 mL) and neutralized with 10% NaOH solution until pH 10. The resulting aqueous layer was extracted with EtOAc (2×30 mL) and the combined organic layers washed with brine, dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated to afford the title compound as a grey solid (0.80 g, 73%). It was used in the next step without purification. MS (ES+): m/z 314 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528143B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-266184dcbe9d48fabbb2b8768a2a1e9c
출처 메모uspto-grants-2009_05