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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470293Generated: October 30, 2026

Triethylamine → 4-[4-Amino-4-(4-tert-butyl-benzyl)-piperidin-1-yl]-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1470293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 53438275—
Reactant4-(4-Tert-butyl-benzyl)-piperidin-4-ylamine hydrochlorideHCID 66872537—
Solvent1-ButanolHCID 263—
Product4-[4-Amino-4-(4-tert-butyl-benzyl)-piperidin-1-yl]-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl esterHCID 5789917865%

Reaction Steps

A mixture of 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid ethyl ester (Example 68A) (50 mg, 0.22 mmol), 4-(4-tert-butyl-benzyl)-piperidin-4-ylamine hydrochloride (70.8 mg, 0.22 mmol) and triethylamine (150 μL) in n-butanol (1.5 mL) was irradiated in a microwave reactor (200 W) for 1 hour at 100° C. After cooling, the solvent was evaporated and the residue was purified by column chromatography (EtOAc-MeOH 4:1) to give an off-white solid (63 mg, 65%). LC-MS (LCT2) m/z 436 [M+H+], Rt 5.01 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006430B2
Source datasetuspto-grants-2015_04
ORD IDord-5f831d1aafff4198b85325167366a9e2
Source noteuspto-grants-2015_04