HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736720Generated: November 1, 2026
Trifluoroacetic acid → HCID 22912861, compound
https://huagongshe.com/reaction/1736720
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Reactant | Tert-butyl 4,5-dihydro-5-[(pyrrolidino)carbonyl]imidazo[1,5-a]quinoxaline-3-carboxylate | HCID 22912827 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 22912861 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05541324 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-856540e26bd447d0998ad5d50bc12fb1 |
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| Source note | uspto-grants-1996_07 |
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