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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394127Generated: November 2, 2026

Trifluoroacetic acid → HCID 18439829, compound

https://huagongshe.com/reaction/1394127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69202883HCID 69202883—
SolventDichloromethaneHCID 6344—
ProductHCID 18439829HCID 1843982995.8%

Reaction Steps

The BOC protecting group was removed by the following procedure. Into a 200 mL round bottom flask equipped with a magnetic stir bar and nitrogen inlet was placed 1.0 g (2.71 mmoles, 1 equiv) of [4-amino-2-(3-chlorophenyl)-quinolin-6-yl]-carbamic acid tert-butyl ester and 60 mL of a 1:2 mixture of trifluoroacetic acid and methylene chloride. The mixture was stirred at room temperature for 3 hrs., then concentrated. The residue was made basic with dilute NaOH solution then extracted with ethyl acetate. The organic layer was washed with NaHO solution, dried over Na2SO4, filtered and concentrated. The residue was crystallized from methylene chloride and hexanes to give 700 mg (95%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348340B2
Source datasetuspto-grants-2008_03
ORD IDord-af627e6a4ae14840861d18b146600f57
Source noteuspto-grants-2008_03