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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657824Generated: October 31, 2026

1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanamine → 2-(4-(1-(4-chloro-3-(methylsulfonyl)phenyl)ethylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-5-methylbenzonitrile

https://huagongshe.com/reaction/657824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanamineHCID 58188171—
Reactant2-(4-Chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-5-methylbenzonitrileHCID 59840688—
SolventAcetonitrileHCID 6342—
SolventDiisopropylethylamineHCID 81531—
Product2-(4-(1-(4-chloro-3-(methylsulfonyl)phenyl)ethylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-5-methylbenzonitrileHCID 25061360—

Reaction Steps

A reaction mixture of 2-(4-chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-5-methylbenzonitrile (250 mg, 0.88 mmol) and 1-(4-chloro-3-(methylsulfonyl)phenyl)ethanamine (300 mg, 1.28 mmol) in acetonitrile (2 mL) and N,N-diisopropylethylamine (700 μL) was subjected to microwave irradiation at 185° C. for 3.5 h. The reaction mixture was concentrated and the residue was purified by preparative HPLC (100×20.2 mm, C18 column; 30-60% acetonitrile-water [10 mM Et2NH]) to afford a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076345B2
Source datasetuspto-grants-2011_12
ORD IDord-71236bf522e8407295a18c0113e6bf02
Source noteuspto-grants-2011_12