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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 507550생성일: 2026년 10월 27일

Morpholine → 2-(Methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidine

https://huagongshe.com/reaction/507550

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물TriethylamineHCID 8471—
반응물5-(2-(Methylthio)-4-pyrimidinyl)-2-thiophenesulfonyl chlorideHCID 2736995—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물2-(Methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidineHCID 6020437873.5%

반응 단계

A mixture of 5-(2-(methylthio)pyrimidin-4-yl)thiophene-2-sulfonyl chloride (200 mg, 0.65 mmol), morpholine (62 mg, 0.72 mmol) and triethylamine (78 mg, 0.78 mmol) in tetrahydrofuran (5 mL) was stirred at rt for 2 days. Water (50 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine (50 mL), dried over anhydrous sodium sulfate and filtered. The solvent was evaporated in vacuo and the residue was washed with diethyl ether (2 mL) to give a white solid. The solid was dissolved in 30 mL of acetone-water (1:1) and then oxone (2 g) was added. After stirring at rt for 20 h the mixture was concentrated in vacuo to remove the acetone. The white precipitate was filtered off, washed with water and dried to afford the title compound (186 mg, 73%). MS (M+H)+ 390.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786132B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8690195d7efc4f38b511169274fd3a82
출처 메모uspto-grants-2010_08