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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187424Generated: November 1, 2026

Trifluoroacetic acid → HCID 22082733, compound

https://huagongshe.com/reaction/2187424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22082763HCID 22082763—
SolventDichloromethaneHCID 6344—
ProductHCID 22082733HCID 2208273370%

Reaction Steps

To an ice-cooled solution of (R)-N-[8-(4-tert-butyloxycarbonylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinophenylcarboxamide (1.0 g, 2 mmol) in methylene chloride (100 mL) was added trifluoroacetic acid (3 mL). The reaction was stirred at ambient temperature for 7 h. The solvent was evaporated in vacuo and the residue was dissolved in water (20 mL), alkalized with a 2 M aqueous sodium hydroxide solution and extracted, twice, with methylene chloride. The phases were separated, the combined organic phases were dried (Na2SO4), filtered and evaporated in vacuo. Purification on a silica gel column using chloroform/methanol/concentrated ammonium hydroxide (95:5:0.5) as the eluent gave 580 mg (70% yield) of the title compound as white crystals: mp 202-203° C.; [α]21D −56° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 420 (5, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-aa03fe5c44a44d6299c16d38c0eb4d13
Source noteuspto-grants-2002_06