Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984313Generated: October 28, 2026

Thiomorpholine → HCID 44409995, compound

https://huagongshe.com/reaction/1984313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
ReactantHCID 10214516HCID 10214516—
SolventDichloromethaneHCID 6344—
ProductHCID 44409995HCID 4440999571%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of thiomorpholine (2.27 g, 22 mmol) and 6-chioro-N,2-dicyclopropyl-5-fluoro-4-pyrimidinamine 31 (1 g, 4.4 mmol) is stirred at 110° C. for 18 hours. After cooling, the brown solution is diluted with dichloromethane, washed two times with a saturated sodium bicarbonate solution. The combined organic layers are dried over magnesium sulfate and concentrated under high vacuum to afford a brown oil. The crude oil is purified by column chromatography (hexane/ethyl acetate: 80/20) to give N,2-dicyclopropyl-5-fluoro-6-(4-thiomorpholinyl)-4-pyrimidinamine 120 (915 mg, 71%) as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544675B2
Source datasetuspto-grants-2009_06
ORD IDord-2c63af0fd1c648dfbf0db312db9fb374
Source noteuspto-grants-2009_06