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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930507Generated: October 26, 2026

Isopropanol → 2-(pyridin-3-ylcarbonyl)-N-3-thienyl-1,2,3,4-tetrahydroisoquinolin-6-amine

https://huagongshe.com/reaction/930507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantEthyl AcetateHCID 8857—
ReactantThiophen-3-amineHCID 640543—
Reactant(2-Chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)(pyridin-3-yl)methanoneHCID 118970896—
Product2-(pyridin-3-ylcarbonyl)-N-3-thienyl-1,2,3,4-tetrahydroisoquinolin-6-amineHCID 11897090739.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of (2-chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)(pyridin-3-yl)methanone, Intermediate 5 (0.025 g, 0.091 mmol) in isopropanol (0.1 mL) was treated with thiophen-3-amine (0.0099 g, 0.100 mmol). The resulting mixture was heated to 60° C. and allowed to stir overnight. After being allowed to cool to room temperature EtOAc (10 mL) was added to the reaction mixture, and the resulting solution was then washed twice with brine (10 mL). The combined aqueous layers were washed once with EtOAc (10 mL). The organic layers were combined, then dried over anhydrous Na2SO4(s), filtered and concentrated in vacuo. The resulting crude residue was then purified over silica using a MeOH/CHCl3 gradient. The desired product was obtained in 39.1% yield (0.012 g, 0.035 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296747B1
Source datasetuspto-grants-2016_03
ORD IDord-3ad152f8abcf4bc2967373e4ba6f2086
Source noteuspto-grants-2016_03