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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294012Generated: October 25, 2026

Triethylamine → 5-(7-benzyloxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine

https://huagongshe.com/reaction/2294012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-5-(chloromethyl)-2-methylpyrimidineHCID 421245—
Reactant7-(Benzyloxy)-1,2,3,4-tetrahydroisoquinolineHCID 21463014—
SolventDimethylformamideHCID 6228—
Product5-(7-benzyloxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamineHCID 2147368551%

Reaction Steps

A suspension of 0.23 g (0.0012 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine in 10 ml of dimethylformamide was treated with 0.42 ml (0.0030 mol) of triethylamine and 0.29 g (0.0012 mol) of 7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline and the mixture was stirred at room temperature under argon for 18 hours. The solvent was distilled off in a high vacuum. The residue was partitioned between dichloromethane/water, extracted and dried over MgSO4. After removing the solvent the residue was chromatographed on silica gel with ethyl acetate as the eluent. 0.22 g (51%) of 5-(7-benzyloxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine was obtained as a colourless solid; m.p. 151°-153°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688798
Source datasetuspto-grants-1997_11
ORD IDord-378920fcdbcd4390a64190d968976ed5
Source noteuspto-grants-1997_11