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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351081Generated: November 2, 2026

Trifluoroacetic acid → HCID 21098120, compound

https://huagongshe.com/reaction/1351081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21098101HCID 21098101—
SolventDichloromethaneHCID 6344—
ProductHCID 21098120HCID 21098120—

Reaction Steps

2 ml of trifluoroacetic acid are added to 220 mg of 2-(4-tert.-butyloxycarbonyl-piperazin-1-yl)-3-(2-butyn-1-yl)-5-[(2,3,8-trimethyl-quinoxalin-6-yl)methyl]-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one in 4 ml methylene chloride. The reaction mixture is stirred for one hour at ambient temperature. Then it is diluted with methylene chloride and washed with saturated sodium hydrogen carbonate solution. The organic phase is dried and evaporated down. The glassy residue is dissolved in dioxane, frozen with liquid nitrogen and dried at 6×10−3 mbar. A white solid remains.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217711B2
Source datasetuspto-grants-2007_05
ORD IDord-4aa02fa9d49541f3a8072ef7df4d5e0f
Source noteuspto-grants-2007_05