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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512116Generated: October 31, 2026

Methanol → HCID 89545461, compound

https://huagongshe.com/reaction/512116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 12514465HCID 12514465—
ReactantMethyl 5-(bromomethyl)-2-fluorobenzoateHCID 22645461—
SolventDimethylformamideHCID 6228—
ProductHCID 89545461HCID 89545461—

Reaction Steps

Similarly, compounds of this invention can be prepared as illustrated by the exemplary reaction in Scheme 2. Reaction of the intermediate 2,4-di(trimethylsiloxy)-5,6,7,8-tetrahydroquinazoline with methyl 5-(bromomethyl)-2-fluorobenzoate in DMF, followed by treatment with 1,4-dioxane and methanol, produced 1-(4-fluoro-3-methoxycarbonylbenzyl)-5,6,7,8-tetrahydroquinazol ine-2,4(1H,3H)-dione. Treatment of the ester with NaOH in water-methanol produced 1-(4-fluoro-3-carboxybenzyl)-5,6,7,8-tetrahydroquinazoline-2,4(1H,3H)-dione. Coupling of the acid with a substituted amine, such as 1-cyclopentylcarbonylpiperazine, in the presence of coupling agents, such as HATU and DIPEA in DMF, produced the targeted compound 1-(4-fluoro-3-(4-(cyclopentylcarbonyl)piperazine-1-carbonyl)benzyl)-5,6,7,8-tetrahydroquinazoline-2,4(1H,3H)-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102631B2
Source datasetuspto-grants-2015_08
ORD IDord-160c86556e424751b835a631beb8141b
Source noteuspto-grants-2015_08