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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507550Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/507550

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
EduktTriethylamineHCID 8471—
Edukt5-(2-(Methylthio)-4-pyrimidinyl)-2-thiophenesulfonyl chlorideHCID 2736995—
EduktPotassium hydroxy sulfiteHCID 23707502—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelPropan-2-one--water (1/1)HCID 18366337—
Produkt2-(Methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidineHCID 6020437873,5%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786132B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-8690195d7efc4f38b511169274fd3a82
Quellennotizuspto-grants-2010_08