Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809753Generated: October 30, 2026

4-Chlorobenzylamine → HCID 178452781, compound

https://huagongshe.com/reaction/1809753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
ReactantHCID 178504618HCID 178504618—
ProductHCID 178452781HCID 178452781—

Reaction Conditions

Temperature130 °C

Reaction Steps

The mixture of {4-[3-(2-methanesulfinyl-pyrimidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (from Example 9 supra) (150 mg, 0.32 mmol) and 4-chlorobenzylamine (179 mg, 1.3 mmol) was heated at 130° C. with stirring for 2 hours. The resulting oil was purified by chromatography (silica gel, 6 g, 200-300 mesh, eluting with dichloromethane:methanol, 50:1 to 30:1) and then further purified by prep-HPLC to afford (4-{3-[2-(4-chloro-benzylamino)-pyrimidin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino}-cyclohexyl)-carbamic acid tert-butyl ester. (Yield 35 mg, 20.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362023B2
Source datasetuspto-grants-2013_01
ORD IDord-71a43d89655f48608e6df68d00a351a6
Source noteuspto-grants-2013_01