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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442998Generated: October 30, 2026

tert-butyl (2R)-2-[({7-(benzyloxy)-4-[3-chloro-4-fluoroanilino]quinazolin-5-yl}oxy)methyl]pyrrolidine-1-carboxylate → HCID 136344272, compound

https://huagongshe.com/reaction/1442998

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (2R)-2-[({7-(benzyloxy)-4-[3-chloro-4-fluoroanilino]quinazolin-5-yl}oxy)methyl]pyrrolidine-1-carboxylateHCID 86607803—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 136344272HCID 136344272—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of tert-butyl (2R)-2-[({7-(benzyloxy)-4-[3-chloro-4-fluoroanilino]-quinazolin-5-yl}oxy)methyl]pyrrolidine-1-carboxylate (230 mg) (obtained as described in Example 16) and 5% palladium on carbon in ethanol (5 ml) was stirred under hydrogen (5 bar pressure) at 25° C. for 16 hours. The mixture was then filtered and concentrated in vacuo to leave the tert-butyl (2R)-2-[({4-[3-chloro-4-fluoroanilino]-7-hydroxyquinazolin-5-yl}oxy)methyl]pyrrolidine-1-carboxylate as a light brown oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659279B2
Source datasetuspto-grants-2010_02
ORD IDord-e2eb935c87d247a4a909488938a299ad
Source noteuspto-grants-2010_02