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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175743Generated: November 1, 2026

Triethylamine → N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1175743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-benzyl-N,4-dimethylpiperidin-3-amineHCID 9943889—
ReactantHCID 178418725HCID 178418725—
ProductN-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 1208482950%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 4-chloropyrrolo[2,3-d]pyrimidine (2.4 grams, 15.9 mmol), prepared by the method of Davoll, J. Am. Chem. Soc., 82, 131 (1960), which is incorporated by reference in its entirety, and the product from Method A (1.7 grams, 7.95 mmol) dissolved in 2 equivalents of triethylamine was heated in a sealed tube at 100° C. for 3 days. Following cooling to room temperature and concentration under reduced pressure, the residue was purified by flash chromatography (silica; 3% methanol in dichloromethane) affording 1.3 grams (50%) of the title compound as a colorless oil. LRMS: 336.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842699B2
Source datasetuspto-grants-2010_11
ORD IDord-4473827dde6f47a7bab6add3dee9d27f
Source noteuspto-grants-2010_11