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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405982Generated: October 31, 2026

Triethylamine → 4-(4-chlorobenzyl)-1-(7H-pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-amine

https://huagongshe.com/reaction/2405982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
Reactant4-(4-Chlorobenzyl)-piperidin-4-ylamine hydrochlorideHCID 66873031—
Solvent1-ButanolHCID 263—
Product4-(4-chlorobenzyl)-1-(7H-pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-amineHCID 1775181949.3%

Reaction Steps

A solution of 4-(4-chlorobenzyl)piperidin-4-yl amine hydrochloride (0.060 g, 0.2016 mmol), 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (0.031 g, 0.2016 mmol) and triethylamine (0.140 ml, 1.0079 mmol) in n-butanol (2.0 ml) was heated to 100° C. for 24 hours. Concentration and purification by preparative silica TLC gave a white solid (0.034 g, 49%). LC-MS (LCT) m/z 342 [M+H+], Rt 3.25 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809336B2
Source datasetuspto-grants-2014_08
ORD IDord-c9c0d31cb26c473ea567fe5288372431
Source noteuspto-grants-2014_08