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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19571생성일: 2026년 10월 23일

N-methyl-2-pyrrolidone → 2-(2-Morpholinoethyl)thieno[2,3-d]pyrimidine

https://huagongshe.com/ko/reaction/19571

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물2-MorpholinoethylamineHCID 408285—
반응물2-(Methylsulfonyl)thieno[2,3-d]pyrimidineHCID 21988356—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(2-Morpholinoethyl)thieno[2,3-d]pyrimidineHCID 6855914287.6%

반응 단계

A solution of 2-(methylsulfonyl)thieno[2,3-d]pyrimidine (1.0 g, 4.67 mmol), 4-(2-aminoethyl)morpholine (1.8 g, 14.02 mmol), and 1-methyl-2-pyrrolidinone (1.5 mL) was heated to 100° C. overnight. The reaction mixture was cooled to RT and diluted with EtOAc (200 mL)/water (75 mL). The layers were separated, and the organic layer was washed successively with water (4×75 mL) and brine (1×75 mL). The organic layer was then dried over MgSO4, filtered and concentrated to give (1.2 g) of the crude product. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 5% to 95% MeOH in DCM to provide the title compound (1.02 g) MS (ES+): 265 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745449B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d2b26d6d89424ae8a6597c6c0ad4a804
출처 메모uspto-grants-2010_06