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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238108Generated: November 1, 2026

Trifluoroacetic acid → HCID 5329049, compound

https://huagongshe.com/reaction/238108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant7-(1-(Tert-butoxycarbonyl)piperidin-4-ylmethoxy)-4-(2-fluoro-4-methylanilino)-6-methoxyquinazolineHCID 10962085—
SolventDichloromethaneHCID 6344—
ProductHCID 5329049HCID 532904987%

Reaction Steps

A suspension of 7-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-4-(2-fluoro-4-methylanilino)-6-methoxyquinazoline (318 mg, 0.64 mmol) in methylene chloride (5 ml) containing TFA (2.5 ml) was stirred at ambient temperature for 2 hours. The volatiles were removed under vacuum and the residue was partitioned between methylene chloride and water. The aqueous layer was adjusted to pH10-11. The organic layer was separated, washed with water, brine, dried (MgSO4) and the volatiles were removed by evaporation to give 4-(2-fluoro-4-methylanilino)-6-methoxy-7-(piperidin-4-ylmethoxy)quinazoline (220 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642608B2
Source datasetuspto-grants-2014_02
ORD IDord-8d06e937daf04b1986411b6ef6e99266
Source noteuspto-grants-2014_02