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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450535생성일: 2026년 10월 25일

2-Methoxyethylamine → 4-(4-Fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenylamino)-N-(2-methoxyethyl)-5-methylthieno[2,3-d]pyrimidine-6-carboxamide

https://huagongshe.com/reaction/450535

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참여 물질

역할이름HCID투입량
반응물2-MethoxyethylamineHCID 8018—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4-[4-Fluoro-2-(tetrahydro-pyran-4-yloxy)-phenylamino]-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylic acid methylesterHCID 46182044—
용매DimethylformamideHCID 6228—
생성물4-(4-Fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenylamino)-N-(2-methoxyethyl)-5-methylthieno[2,3-d]pyrimidine-6-carboxamideHCID 4618204250.4%

반응 조건

온도0 °C

반응 단계

HATU (0.052 g, 0.138 mmol) was added into a mixture of methyl 4-(4-fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenylamino)-5-methylthieno[2,3-d]pyrimidine-6-carboxylate (0.050 g, 0.125 mmol) and Hünig's base (22 μL, 0.125 mmol) in DMF (2.0 mL) at 0° C. The reaction mixture was stirred at 0° C. for 0.5 hours. 2-Methoxyethylamine (54.3 μL, 0.625 mmol) was added and the coolant removed. The reaction mixture was stirred at ambient temperature overnight. The product was purified by reverse phase preparative HPLC to yield white solid (0.029 g, 50%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486953B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-960802d9ccd848949415e3207e830ff3
출처 메모uspto-grants-2013_07