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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216032Generated: October 29, 2026

Triethylamine → 4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4yl)-piperidine-4-carboxylic acid

https://huagongshe.com/reaction/216032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-5-methyl-7H-pyrrolo(2,3-d)pyrimidineHCID 14809282—
Reactant4-Methylpiperidine-4-carboxylic acid hydrochlorideHCID 51000379—
SolventIsopropanolHCID 3776—
Product4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4yl)-piperidine-4-carboxylic acidHCID 6703678193.4%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of 4-chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine (0.274 g, 1.64 mmol) in isopropanol (10 mL) were added 4-methylpiperidine 4-carboxylic acid hydrochloric acid from step A (0.294 g, 1.64 mmol) and triethylamine (0.654 mL, 4.92 mmol). The reaction was heated to 180° C. for 1 hour under microwave conditions, concentrated, taken up with ice water, and neutralized to pH 3 with 6 N aq. HCl to precipitate the product. The product was collected by filtration and dried under vacuum overnight to give the title compound (0.42 g, 75%) as a gray solid. MS (ES+) [M+H]+=275.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193202B2
Source datasetuspto-grants-2012_06
ORD IDord-19066ba6d4d64d8b95399f779f2e9401
Source noteuspto-grants-2012_06