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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845722Generated: November 2, 2026

Trifluoroacetic acid → HCID 57568679, compound

https://huagongshe.com/reaction/1845722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 68924304HCID 68924304—
SolventDichloromethaneHCID 6344—
ProductHCID 57568679HCID 5756867956.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic acid (8 mL) was added to a 0° C. solution of N-(2-{2-[2-(2-{[4-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]oxy}ethoxy)ethoxy]ethoxy}ethyl)-3-(tritylthio)propanamide (1.38 g, 1.65 mmol) and triethylsilane (3.16 mL, 19.8 mmol) in dichloromethane (12 mL). The solution was stirred at 0° C. for 2 hours, then was concentrated under reduced pressure. The residue was concentrated under reduced pressure from toluene several times. The crude product was purified twice by HPFC on silica gel (gradient elution with 2-70% CMA in chloroform) to provide 0.55 g of N-(2-{2-[2-(2-{[4-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]oxy}ethoxy)ethoxy]ethoxy}ethyl)-3-mercaptopropanamide as a foam. MS (ESI) m/z 594 (M+H)+. Anal. Calcd for C28H43N5O7S: C, 56.64; H, 7.30; N, 11.80; S, 5.40. Found: C, 56.36; H, 7.52; N, 11.53; S, 5.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951528B2
Source datasetuspto-grants-2015_02
ORD IDord-88a42d5a5c554f18a51bebfd23db9de9
Source noteuspto-grants-2015_02