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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346562Generated: October 30, 2026

Trifluoroacetic acid → HCID 5329049, compound

https://huagongshe.com/reaction/346562

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 pH 10–11. 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 numberUS07173038B1
Source datasetuspto-grants-2007_02
ORD IDord-eb1727bd4c084601b751586944ed290c
Source noteuspto-grants-2007_02