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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098375Generated: October 25, 2026

Pyridine → N-(3-tert-butylphenyl)-4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide

https://huagongshe.com/reaction/2098375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant3-tert-ButylanilineHCID 79334—
Reactant1-[(Tert-butoxy)carbonyl]-4-methylpiperidine-4-carboxylic acidHCID 23282848—
ReactantHCID 86635224HCID 86635224—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
ProductN-(3-tert-butylphenyl)-4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamideHCID 5792020061%

Reaction Steps

Preparation of tert-Butyl 4-(3-tert-butylphenylcarbamoyl)-4-methylpiperidine-1-carboxylate. To a solution of 1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (0.30 g, 1.2 mmol), DMF (20 drops), and pyridine (0.38 g, 4.8 mmol) in dichloroethane (10 mL) was added oxalyl chloride (0.15 g, 1.2 mmol). The mixture was stirred for 40 minutes, and 3-tert-butylaniline was added. The mixture was stirred for 1 hour, diluted with dichloromethane, washed twice each with sat. aq. NaHCO3 and 1.0 N aq. HCl, dried over MgSO4, and concentrated. Silica gel chromatography (0-2% MeOH:CH2Cl2) gave the title compound in 61% yield. MS (ES+) [M+H]+375.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450332B2
Source datasetuspto-grants-2013_05
ORD IDord-ed7a01bbd0af4d918e25666e97d4466e
Source noteuspto-grants-2013_05