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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452651Generated: November 2, 2026

Trifluoroacetic acid → HCID 10023999, compound

https://huagongshe.com/reaction/1452651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57526952HCID 57526952—
SolventDichloromethaneHCID 6344—
ProductHCID 10023999HCID 1002399999.9%

Reaction Steps

Into a solution of tert-butyl 4-(3-{[6-(3,4-difluoroanilino)hexanoyl]amino}phenyl)-1-piperidine carboxylate (11.2 mg, 0.0224 mmol) in dichloromethane (0.500 mL) at 0° C. was slowly added trifluoroacetic acid (25.5 mg, 2.24 mmol). The reaction mixture was stirred at room temperature for 10 min and concentrated in vacuo. The residue was dissolved in i-PrOH/CHCl3 (1:3, 10 mL) and basified to pH 11 with 10% KOH, washed with H2O, followed by brine. The organic layer was dried over MgSO4 and concentrated in vacuo to give the desired product (8.98 mg, 99%): 1H NMR (400. MHz, CDCl3) δ 7.39-7.08 (m, 5H), 7.06-6.94 (m, 2H), 6.91-6.81 (m, 1H), 6.77-6.67 (m, 1H), 3.54-3.42 (m, 2H), 3.25-3.04 (m, 3H), 2.91-2.80 (m, 1H), 2.45-2.32 (m, 2H), 2.11-1.99 (m, 2H), 1.98-1.83 (m, 2H), 1.80-1.62 (m, 4H), 1.55-1.40 (m, 2H), 1.34-1.23 (m, 1H); ESMS m/e: 402.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473698B2
Source datasetuspto-grants-2009_01
ORD IDord-4c467d23442146c18b0a79231fb74d32
Source noteuspto-grants-2009_01