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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868452Generated: November 1, 2026

Thiomorpholine → HCID 57982502, compound

https://huagongshe.com/reaction/1868452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
ReactantHCID 57982522HCID 57982522—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57982502HCID 5798250291.3%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirred solution of methyl 2-bromo-7-(2,4-dichlorophenyl)-5-methyl-[1,2,4]-triazolo[1,5-a]pyrimidine-6-carboxylate (30 mg, 0.07 mmol) in dioxane (2 mL) was added thiomorpholine (15 μL, 0.14 mmol). After heating to 75° C. for 16 h, the reaction was concentrated under reduced pressure and diluted with EtOAc. The organic layer was washed with satd aq NH4Cl and brine prior to drying over anhydrous MgSO4. Filtration, concentration under reduced pressure and purification by silica gel chromatography afforded methyl 7-(2,4-dichlorophenyl)-5-methyl-2-thiomorpholino-[1,2,4]-triazolo[1,5-a]pyrimidine-6-carboxylate (28 mg, 90%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635699B2
Source datasetuspto-grants-2009_12
ORD IDord-73ff50dd2fb9452b85812dabdecb2fb5
Source noteuspto-grants-2009_12