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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472627Generated: November 1, 2026

Dimethylformamide → HCID 86711139, compound

https://huagongshe.com/reaction/1472627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21185174HCID 21185174—
ReactantHCID 136377194HCID 136377194—
SolventAcetoneHCID 180—
ProductHCID 86711139HCID 86711139—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 9-((tert-butyldimethylsilyl)oxy)-3-(2-(4-(6-hydroxybenzo[d]isoxazol-3-yl)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one, prepared as described in the previous step, (50 mg, 0.093 mmol) in acetone (0.5 mL) and DMF (0.5 mL) was treated with potassium carbonate (33.3 mg, 0.24 mmol) and N-Boc-2-bromoaminoethane (27 mg, 0.12 mmol), and the reaction mixture was stirred for 17 h at 60° C. under argon. The reaction mixture was evaporated at 40° C. under reduced pressure and dissolved in water (10 mL) and extracted with dichloromethane (3×10 mL). The organic layers were combined, dried over Na2SO4, filtered, and the solvent was evaporated yield the crude title compound. (ESI-MS (M+1) 682)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012648B2
Source datasetuspto-grants-2015_04
ORD IDord-444013ff185d47149d1ebf14f596949a
Source noteuspto-grants-2015_04