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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364020Generated: October 30, 2026

Trifluoroacetic acid → HCID 66958560, compound

https://huagongshe.com/reaction/1364020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66958543HCID 66958543—
SolventDichloromethaneHCID 6344—
ProductHCID 66958560HCID 66958560—

Reaction Steps

Trifluoroacetic acid (500 mL of a 10% solution in dichloromethane) was added to tert-butyl 11-{[tert-butyl(dimethyl)silyl]oxy}-11,12-dihydro-8H-[1,4]diazepino[1′,2′:1,2]imidazo[4,5-c]quinoline-9(10H)-carboxylate (9.23 g, 19.7 mmol), and the reaction was stirred at ambient temperature for 75 minutes. The solvent was removed under reduced pressure, and the residue was shaken with triethylamine (300 mL) and dichloromethane. The solution was concentrated under reduced pressure, and the product was dried under high vacuum for two hours to provide 11-{[tert-butyl(dimethyl)silyl]oxy}-9,10,11,12-tetrahydro-8H-[1,4]diazepino[1′,2′:1,2]imidazo[4,5-c]quinoline, which was used in the next step without removing the triethylamine trifluoroacetate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888349B2
Source datasetuspto-grants-2011_02
ORD IDord-9fd1a14c7c264511b6cb3950eda38032
Source noteuspto-grants-2011_02