Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172334Generated: October 31, 2026

Hydrochloric Acid → 4-(2-Methoxy-4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine hydrochloride

https://huagongshe.com/reaction/2172334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Methoxy-4-(trifluoromethyl)phenyl)boronic acidHCID 24901776—
Reactanttert-butyl 4-chloro-5H,6H,7H,8H-pyrido(3,4-d)pyrimidine-7-carboxylateHCID 52987620—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product4-(2-Methoxy-4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine hydrochlorideHCID 89813768104%

Reaction Steps

A solution of PdCl2(dppf)-CH2Cl2 adduct (0.091 g, 0.111 mmol), (2-methoxy-4-(trifluoromethyl)phenyl)boronic acid (0.815 g, 3.71 mmol), tert-butyl 4-chloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate (1.000 g, 3.71 mmol), and potassium carbonate (2.050 g, 14.83 mmol) in 12 mL of dioxane and 4 mL water was heated to 110° C. for one hour. The reaction mixture was then diluted with DCM, the organics were dried over MgSO4 and concentrated. The crude residue was treated with HCl (4N in dioxane) (9.27 ml, 37.1 mmol) and was allowed to stir at room temperature overnight. The reaction mixture was diluted with ether, and the resulting solids were filtered off and dried yielding 4-(2-methoxy-4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine hydrochloride (1.333 g, 3.86 mmol, 104% yield) as a gray solid with minor impurities. (M+H)+=310.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051311B2
Source datasetuspto-grants-2015_06
ORD IDord-60952c7f7835494e8ef7be51ffe45a73
Source noteuspto-grants-2015_06