HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715486Generated: October 25, 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/reaction/715486
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Alaninol | HCID 80307 | — |
| Reactant | 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 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 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% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187475B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7ceb700fbfbb4ff9b1fdcf5ff47e3e80 |
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| Source note | uspto-grants-2015_11 |
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