HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895673Generated: October 31, 2026
Trifluoroacetic acid → HCID 59548955, compound
https://huagongshe.com/reaction/1895673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57518484 | HCID 57518484 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59548955 | HCID 59548955 | 76.4% |
Reaction Steps
(R)-[3-(1-Ethylcarbamoyl-3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazin-7-yl)-3-oxo-1-(2,4,5-trifluoro-benzyl)-propyl]-carbamic acid tert-butyl ester 42a (190 mg, 0.33 mmol) was dissolved in 10 mL of dichloromethane, and trifluoroacetic acid (750 mg, 6.6 mmol) was added to the solution. The reaction mixture was stirred at room temperature for 2 hours and monitored by thin layer chromatography until the disappearance of the starting materials. The reaction mixture was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound (R)-7-[3-amino-4-(2,4,5-trifluoro-phenyl)-butyryl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylic acid ethylamide 42 (120 mg, yield 76.4%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513411B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-e9564964f71849888111ec8b0ae8749e |
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| Source note | uspto-grants-2013_08 |
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