HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 715486Erstellt: 24. Oktober 2026
L-Alaninol → N-((S)-1-hydroxypropan-2-yl)-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxamide
https://huagongshe.com/de/reaction/715486
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | L-Alaninol | HCID 80307 | — |
| Edukt | phenyl 2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxylate | HCID 89875412 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-((S)-1-hydroxypropan-2-yl)-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxamide | HCID 89874554 | 52% |
Reaktionsschritte
A mixture of phenyl 2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxylate (20 mg, 0.042 mmol, Intermediate-91, single enantiomer) and (S)-2-aminopropan-1-ol in THF (1.0 mL) is heated at 90° C. overnight. The reaction mixture is concentrated. The residue is purified by preparative LC-MS to give 9.9 mg (52% yield) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09187475B2 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-7ceb700fbfbb4ff9b1fdcf5ff47e3e80 |
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| Quellennotiz | uspto-grants-2015_11 |
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