Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732961Generated: October 30, 2026

Thiomorpholine → HCID 57839070, compound

https://huagongshe.com/reaction/732961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
ReactantHCID 57839059HCID 57839059—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57839070HCID 57839070101.8%

Reaction Steps

To a stirred solution of methyl 2-(benzylsulfonyl)-4-(2,4-dichlorophenyl)-6-methylpyrimidine-5-carboxylate (17 mg, 0.037 mmol) in dioxane (2 mL) was added thiomorpholine (4.5 mL, 0.045 mmol). After at 40° C. for 1 hr, the reaction was concentrated under reduced pressure and diluted with EtOAc (10 mL). The organic layer was extracted with saturated NaHCO3 solution (2×6 mL), brine (5 mL), dried (MgSO4), filtered and concentrated under reduced pressure to give methyl 4-(2,4-dichlorophenyl)-6-methyl-2-thiomorpholinopyrimidine-5-carboxylate (15 mg, 100%). The crude reaction product (>98% purity) was moved onto next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589088B2
Source datasetuspto-grants-2009_09
ORD IDord-b71d6555c1474e0ab24c1a74475e59f9
Source noteuspto-grants-2009_09