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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809783Generated: October 31, 2026

Benzenemethanamine, 3-chloro- → HCID 178452779, compound

https://huagongshe.com/reaction/1809783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanamine, 3-chloro-HCID 77802—
ReactantHCID 178504618HCID 178504618—
ProductHCID 178452779HCID 178452779—

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 19 supra) (300 mg, 0.64 mmol) and 3-chlorobenzylamine (360 mg, 2.54 mmol) was heated at 130° C., with stirring for 2 hours. The resulting oil was purified by chromatography (silica gel, 10 g, 200-300 mesh, eluting with dichloromethane:methanol, 30:1 to 10:1) to afford (4-{3-[2-(3-chloro-b enzylamino)-pyrimidin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino}-cyclohexyl)-carbamic acid tert-butyl ester. (Yield 150 mg, 43.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362023B2
Source datasetuspto-grants-2013_01
ORD IDord-d04c13c5e90e4187802e67eaa87cad71
Source noteuspto-grants-2013_01