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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416903Generated: November 4, 2026

3-Benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione → 1-Ethyl-5,6,8-trifluoro-3-hydroxy-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione

https://huagongshe.com/reaction/2416903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dioneHCID 22632997—
ReactantHCID 178525683HCID 178525683—
SolventTrifluoroacetic acidHCID 6422—
Product1-Ethyl-5,6,8-trifluoro-3-hydroxy-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dioneHCID 2263299492.8%

Reaction Steps

A solution of 3-benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione (Example X-3, 0.15 g, 0.36 mmol) in trifluoroacetic acid (5.0 mL) was reacted with a 1.0 M solution of boron tris(trifluoroacetate) (1.8 mL, 1.8 mmol) in TFA and allowed to stir for 1 hour. The mixture was then concentrated and the residue dissolved in methanol and concentrated. This process was repeated three times. The residue was then triturated from diethyl ether and filtered to provide 0.11 g of the title compound as a solid, mp 223-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825199B2
Source datasetuspto-grants-2004_11
ORD IDord-cb99553ab4fe461faf2dbc042f93cead
Source noteuspto-grants-2004_11