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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171822Generated: November 1, 2026

Pyridine → HCID 118024110, compound

https://huagongshe.com/reaction/2171822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 118023960HCID 118023960—
SolventWaterHCID 962—
ProductHCID 118024110HCID 118024110—

Reaction Steps

To a mixture of N-{[6-(4,4-dimethylcyclohexyl)-2-methylthieno[2,3-d]pyrimidin-4-yl]methyl}tetrahydro-2H-pyran-4-amine (60 mg), pyridine (129 μL), and DCM (1.8 mL) was added acetic anhydride (76 μL), followed by stirring at room temperature for 30 minutes. To the reaction mixture was added water, followed by extraction with EtOAc. The organic layer was washed with brine, dried over Na2SO4, and then concentrated under reduced pressure. The residue was purified by silica gel column to obtain N-{[6-(4,4-dimethylcyclohexyl)-2-methylthieno[2,3-d]pyrimidin-4-yl]methyl}-N-(tetrahydro-2H-pyran-4-yl)acetamide (23 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051339B2
Source datasetuspto-grants-2015_06
ORD IDord-ddb6b3bca846483283b06a4618475ff4
Source noteuspto-grants-2015_06