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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60512Generated: October 26, 2026

5-(1-hydroxy-3-methylbutyl)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy) propyl)-6-(3-(trifluoromethyl)phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione → HCID 118875892, compound

https://huagongshe.com/reaction/60512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(1-hydroxy-3-methylbutyl)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy) propyl)-6-(3-(trifluoromethyl)phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 118875554—
CatalystZincHCID 23994—
SolventFormic AcidHCID 284—
ProductHCID 118875892HCID 11887589257.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 5-(1-hydroxy-3-methylbutyl)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy) propyl)-6-(3-(trifluoromethyl)phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (60 mg, 0.106 mmol) in HCOOH (5 mL) was added Zn dust (34.7 mg, 0.53 mmol). The reaction was heated at 50° C. for 2 h, cooled to RT and filtered. The filtrate was concentrated and dried to give 3-(5-isopentyl-1-methyl-2,4-dioxo-6-(3-(trifluoromethyl)phenoxy)-1,2-dihydropyrido[2,3-d]pyrimidin-3(4H)-yl)propyl formate (30 mg, 57.3% yield) as a solid. LCMS: MH+ 494 and TR=2.193 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440972B2
Source datasetuspto-grants-2016_09
ORD IDord-545cc902918745a997a5cd92b3882f68
Source noteuspto-grants-2016_09