Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241878Generated: November 1, 2026

Diisopropylethylamine → [6-(5-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-[(S)-cyclopropyl-(6-trifluoromethyl-pyridin-3-yl)-methyl]-amine

https://huagongshe.com/reaction/241878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-6-(5-chloropyridin-2-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidineHCID 58103575—
Reactant(S)-cyclopropyl(6-(trifluoromethyl)pyridin-3-yl)methanamine dihydrochlorideHCID 66871392—
SolventAcetonitrileHCID 6342—
Product[6-(5-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-[(S)-cyclopropyl-(6-trifluoromethyl-pyridin-3-yl)-methyl]-amineHCID 2503357812.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a stirred solution of (S)-cyclopropyl(6-(trifluoromethyl)pyridin-3-yl)methanamine dihydrochloride (0.048 g, 0.17 mmol) and N,N-diisopropylethylamine (96 uL, 0.55 mmol) in acetonitrile (1.8 mL) was added 4-bromo-6-(5-chloropyridin-2-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine (0.045 g, 0.14 mmol). The reaction was heated in microwave for 7 hours at 180° C. The mixture was concentrated and the residue was purified by silica gel column followed by semi-prep HPLC to obtain 7.8 mg of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653091B2
Source datasetuspto-grants-2014_02
ORD IDord-edc55f4eb84747b4bfefa912a5aa58cb
Source noteuspto-grants-2014_02