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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931709Generated: November 2, 2026

Water → HCID 25122893, compound

https://huagongshe.com/reaction/1931709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantButyl chloroformateHCID 61140—
ReactantHCID 44622155HCID 44622155—
SolventDichloromethaneHCID 6344—
ProductHCID 25122893HCID 25122893—

Reaction Steps

A solution of 4-[4-(2-methyl-pyridin-3-yloxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (Example 92; 50 mg, 0.12 mmol) in a mixture of trifluoroacetic acid (0.5 mL) and dichloromethane (2 mL) was stirred at room temperature for 30 min, then the solvents were evaporated under vacuum. Dichloromethane (4 mL) was added, followed successively by n-butyl chloroformate (24 μL, 0.18 mmol) and triethylamine (110 μL, 0.8 mmol). The mixture was stirred overnight at room temperature. Water was added and the mixture was extracted with three times with dichloromethane. The combined dichloromethane layers were evaporated and the residue was purified by C18 reversed phase HPLC using a gradient of 10-100% acetonitrile/water to give 4-[4-(2-methyl-pyridin-3-yloxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid benzyl ester (24 mg) as a waxy solid. 1H NMR showed that this material contained almost one mole equivalent of triethylamine hydrochloride. HRMS Calcd. For C21H27N6O3 (MH+): 411.2139. Found: 411.2139.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188098B2
Source datasetuspto-grants-2012_05
ORD IDord-c1cc3856ba964092958dcc89c3bdfde5
Source noteuspto-grants-2012_05