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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1396729생성일: 2026년 10월 27일

Diisopropylethylamine → 5-Amino-2-[2-(4-fluorophenyl)ethyl]-7-(4-benzoylpiperidine-1-yl)-thiazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/1396729

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Benzoylpiperidine hydrochlorideHCID 2724437—
반응물2-(4-Fluorophenethyl)-7-(methylsulfonyl)thiazolo[5,4-d]pyrimidin-5-amineHCID 50941867—
용매AcetonitrileHCID 6342—
생성물5-Amino-2-[2-(4-fluorophenyl)ethyl]-7-(4-benzoylpiperidine-1-yl)-thiazolo[5,4-d]pyrimidineHCID 4691685091.3%

반응 단계

To a solution of 5-amino-2-[2-(4-fluorophenyl)ethyl]-7-methanesulfonyl-thiazolo[5,4-d]pyrimidine (50 mg, 0.14 mmol) in acetonitrile (5 ml) was added diisopropylethylamine (0.45 mmol, 74 μL) and 4-benzoylpiperidine hydrogen chloride (0.15 mmol). The reaction mixture was stirred at room temperature for 16 hours whereupon the solvent was removed in vacuo. The resulting residue was purified by flash chromatography on silica, the mobile phase being a mixture of methanol and dichloromethane (in a ratio gradually ranging from 100% CH2Cl2 to 1% CH3OH in CH2Cl2), yielding the pure title compound (59 mg) which was characterized by its mass spectrum: MS m/z (%): 462 ([M+H]+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901132B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-63e976ed24c6497bb1580cd398a28e5f
출처 메모uspto-grants-2014_12