Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027955Generated: November 2, 2026

Hydrochloric Acid → n-(4-(5-Methylaminomethyl-1-(2,6-difluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxo-3-(4-methoxyphenyl)thieno[2,3-d]pyrimidin-6-yl)phenyl)-n'-methoxyureahydrochloride

https://huagongshe.com/reaction/1027955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 86620014HCID 86620014—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Productn-(4-(5-Methylaminomethyl-1-(2,6-difluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxo-3-(4-methoxyphenyl)thieno[2,3-d]pyrimidin-6-yl)phenyl)-n'-methoxyureahydrochlorideHCID 8715567396%

Reaction Steps

A mixed solution of N-(4-(5-((benzyl(methyl)amino)methyl)-1-(2,6-difluorobenzyl)-3-(4-methoxyphenyl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl)phenyl)-N′-methoxyurea (2.0 g, 2.87 mmol) synthesized in Reference Example 19, 10%-palladium-carbon (200 mg), 1N hydrochloric acid (3 ml) in ethanol (40 ml) was stirred under hydrogen atmosphere at room temperature for 72 hours. The reaction mixture was subjected to filtration and the filtrate was concentrated to dryness to give the title compound (1.77 g, 96%) as white powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735401B2
Source datasetuspto-grants-2014_05
ORD IDord-eb0b4abd89084c26bdf3969ce8002efb
Source noteuspto-grants-2014_05