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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736720Generated: November 1, 2026

Trifluoroacetic acid → HCID 22912861, compound

https://huagongshe.com/reaction/1736720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantTert-butyl 4,5-dihydro-5-[(pyrrolidino)carbonyl]imidazo[1,5-a]quinoxaline-3-carboxylateHCID 22912827—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 22912861HCID 22912861—

Reaction Steps

To tert-butyl 4,5-dihydro-5-[(pyrrolidino)carbonyl]imidazo[1,5-a]quinoxaline-3-carboxylate (I, EXAMPLE 217, 2.97 g) are added 20 ml of a solution of trifluoroacetic acid and dichloromethane (1/1). After stirring for 3.5 hr an additional 2 ml of the trifluoroacetic acid/dichloromethane solution are added, followed an hour later by another 2 ml and 30 min later with a final 2 ml of the trifluoroacetic acid/dichloromethane solution. The reaction is stirred additional hours and then concentrated under reduced pressure. Dichloromethane is added to the residue and the mixture is again concentrated to give the title compound, which is crystallized from methanol/dichloromethane, mp 197°-200°; MS (m/z) at 312; NMR (DMSO-d6) 1.72, 3.15, 4.86, 7.18-7.22, 7.33, 7.90, 8.70 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541324
Source datasetuspto-grants-1996_07
ORD IDord-856540e26bd447d0998ad5d50bc12fb1
Source noteuspto-grants-1996_07