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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44832생성일: 2026년 10월 24일

Dimethylformamide → (R)-2-(1-(8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)-1H-imidazol-4-yl)acetonitrile

https://huagongshe.com/ko/reaction/44832

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Cesium carbonateHCID 10796—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
반응물HCID 178510863HCID 178510863—
생성물(R)-2-(1-(8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)-1H-imidazol-4-yl)acetonitrileHCID 58405740—

반응 조건

온도110 °C

반응 단계

A mixture of intermediate B (150 mg, 0.509 mmol), 2-(1H-imidazol-4-yl)acetonitrile (1.01 mmol, 2 equivalents, 108 mg), Cut (0.1 equivalents, 0.0509 mmol, 10 mg), trans-1,2 bis(methylamino)cyclohexane (14 mg, 0.102 mmol) and Cs2CO3 (1.01 mmol, 331 mg) in DMF (1 mL) was purged with nitrogen and was subsequently heated in a sealed vial at 110° C. for 18 h. The reaction was diluted with ethyl acetate, filtered through Celite and evaporated. The residue was purified by reverse phase preparative HPLC and lyophilized to give the title compound (185 mg). 1H NMR (CDCl3) δ: 8.66 (s, 1H), 7.91 (s, 1H), 7.76 (s, 1H), 4.31-4.37 (m, 2H), 3.91 (s, 2H), 3.38 (s, 3H), 1.70-2.13 (m, 10H), and 0.93 ppm (t, J=7.4 Hz, 3H); LCMS: 366.1 m/z (M+H)+; ret. Time: 3.444 min (Analytical Method A).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541418B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8cc89f87399b4b3e82cd973d4487ed03
출처 메모uspto-grants-2013_09