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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472738Generated: October 31, 2026

Trifluoroacetic acid → {1-[(5-Chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-pyrido[3,2-d]pyrimidin-3-yl}-acetic acid

https://huagongshe.com/reaction/472738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant{1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-pyrido[3,2-d]pyrimidin-3-yl}-acetic acid tert-butyl esterHCID 68589926—
SolventDichloromethaneHCID 6344—
Product{1-[(5-Chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-pyrido[3,2-d]pyrimidin-3-yl}-acetic acidHCID 59317706—

Reaction Steps

A stirring solution of {1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-pyrido[3,2-d]pyrimidin-3-yl}-acetic acid tert-butyl ester (Intermediate R) (22.1 mg, 0.044 mmol) in DCM (1 ml) is treated with TFA (1 ml). The reaction mixture is stirred at RT and monitored by HPLC/LCMS until the starting material is consumed. After 3 hours, the reaction mixture is diluted with a minimal amount of DCM and concentrated in vacuo. The residue is taken up in a minimal amount of MeOH, concentrated in vacuo, the again in a minimal amount of EtOAc and concentrated in vacuo to afford the title compound as an off white solid; [M+H]+ 449

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633211B2
Source datasetuspto-grants-2014_01
ORD IDord-7444cbe4352f474b8204fd53bf0d6fed
Source noteuspto-grants-2014_01