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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219964Generated: November 3, 2026

Diisopropylethylamine → N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-2-(methoxymethyl)pyrido[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/2219964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant7-Benzyl-N-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-2-(methoxymethyl)pyrido[3,4-d]pyrimidin-4-amineHCID 12004393—
Solvent1,2-DichloroethaneHCID 11—
ProductN-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-2-(methoxymethyl)pyrido[3,4-d]pyrimidin-4-amineHCID 59021578—

Reaction Conditions

Temperature60 °C

Reaction Steps

1-Chloroethyl chloroformate (543 mg, 3.8 mmol) was added dropwise to the solution of 7-benzyl-N-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-2-(methoxymethyl)pyrido[3,4-d]pyrimidin-4-amine from Example 31 (820 mg, 1.9 mmol) and diisopropylethyl amine (490 mg, 3.8 mmol) in 1,2-dichloroethane (5 mL, anhydrous) at room temperature. After addition, the reaction mixture was stirred at 60° C. for 2 h in the atmosphere of nitrogen. Solvent was removed in vacuo, residue was dissolved in methanol (10 mL) and was stirred at 60° C. for 1 hr. Solvent was removed in vacuo, residue was dissolved in ethyl acetate and was washed by sodium bicarbonate aqueous solution, brine and dried over sodium sulfate. Solvent was removed in vacuo and light orange oily residue was directly taken to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414131B2
Source datasetuspto-grants-2008_08
ORD IDord-f6e30175f127424789164b1090022f93
Source noteuspto-grants-2008_08