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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890736Generated: October 31, 2026

p-Toluenesulfonic acid → 7-Benzyl-N-(3-(isoquinolin-3-yl)-4-methylphenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1890736

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant7-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidineHCID 21958838—
Reactant3-(Isoquinolin-3-yl)-4-methylanilineHCID 58317885—
SolventIsopropanolHCID 3776—
Product7-Benzyl-N-(3-(isoquinolin-3-yl)-4-methylphenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amineHCID 58317958—

Reaction Steps

To a reaction vessel containing 7-benzyl-4-chloro-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine (518 mg, 2 mmol), 3-(isoquinolin-3-yl)-4-methylaniline (470 mg, 2 mmol), pTSA (144 mg, 0.6 mmol) is added isopropanol (7 ml). The vessel is purged with nitrogen, sealed. The reaction vessel is placed in a microwave reactor and irradiated for 30 minutes at 130° C. The reaction mixture is cooled to room temperature and diluted with ethyl acetate. It is washed with saturated aqueous NaHCO3, water and brine, dried over anhydrous MgSO4 and concentrated. The residue is subjected to silica gel flash chromatography (2% methanol in dichloromethane) to afford 7-Benzyl-N-(3-(isoquinolin-3-yl)-4-methylphenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amine as a brown solid. LC-MS m/z: 458.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507491B2
Source datasetuspto-grants-2013_08
ORD IDord-1a14e5057a7746249edebdf8bc5c2ed3
Source noteuspto-grants-2013_08