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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168246Generated: October 30, 2026

N-Methyl-N-(piperidin-4-yl)benzamide → HCID 57382935, compound

https://huagongshe.com/reaction/2168246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-N-(piperidin-4-yl)benzamideHCID 12641853—
Reactant4-Chloro-5-methyl-7H-pyrrolo(2,3-d)pyrimidineHCID 14809282—
SolventEthanolHCID 702—
ProductHCID 57382935HCID 57382935—

Reaction Conditions

Temperature150 °C

Reaction Steps

To 4-chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine D4 (0.154 g) and N-methyl-N-4-piperidinylbenzamide D15 (0.2 g) was added Ethanol (5 mL) and the reaction was heated at 150° C. for 30 minutes in the microwave. The reaction was heated again at 150° C. for 20 minutes. During the cooling, a white precipitate formed. This precipitate was filtered off and washed with Ethanol before being dried in vacuo at 40° C. to afford product in 49 mg. The filtrate was removed in vacuo and the crude residue purified by MDAP using the formic acid method. Fractions corresponding to the desired product were combined and solvent removed to give the product E32 in 22 mg. LCMS [M+H][email protected] min (2 min run)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045485B2
Source datasetuspto-grants-2015_06
ORD IDord-b826695ba6424ccd9e725ad8299be6a5
Source noteuspto-grants-2015_06