HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713364Generated: November 2, 2026
HCID 131734051, compound → Trifluoroacetic acid
https://huagongshe.com/reaction/713364
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131734051 | HCID 131734051 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Trifluoroacetic acid | HCID 6422 | 425.7% |
| Product | HCID 118159134 | HCID 118159134 | — |
Reaction Steps
A solution of (R)-6-benzyl-N-(sec-butyl)-2-(4-(2,4-difluorophenoxyl)piperidin-1-yl)-5,6,7,8-tetrahydropyrido[3,4-b]pyrazin-3-amine TFA salt (174.6 mg, 0.281 mmol) in THF (2.81 mL) was treated with Pd(OH)2 (20 wt %, 59.2 mg, 0.084 mmol). Hydrogen gas (balloon) was bubbled through the reaction mixture for 5 min. The vent needle was removed and the reaction was allowed to stir at room temperature under hydrogen atmosphere for 1 h. The reaction mixture was opened to air and filtered through a pad of Celite™, eluting with EtOAcMeOH. The filtrate was collected and concentrated under reduced pressure to give (R)—N-(sec-butyl)-2-(4-(2,4-difluorophenoxyl)piperidin-1-yl)-5,6,7,8-tetrahydropyrido[3,4-b]pyrazin-3-amine as a TFA salt (136.4 mg) as a yellow oil, which was carried forward without additional purification. ESI-MS m/z [M+H]+ 418.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181249B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-26dd88d413cb44a2b3a7c6a1f94ee8f8 |
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| Source note | uspto-grants-2015_11 |
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