HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245702Generated: October 29, 2026
Sodium borohydride → HCID 59216527, compound
https://huagongshe.com/reaction/2245702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59216437 | HCID 59216437 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59216527 | HCID 59216527 | 80% |
Reaction Steps
2-[6-(1-Difluoromethyl-cyclopropyl)-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl]-6-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-benzaldehyde (0.025 g, 0.038 mmole) was dissolved into THF (2 ml). To this solution was added NaBH4 (0.006 g, 0.015 mmole) and the mixture stirred at room temperature 0.5 hour after which it was quenched with ice water (4 ml) and extracted with ethylacetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by preparative TLC to afford 6-(1-Difluoromethyl-cyclopropyl)-2-(2-hydroxymethyl-3-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-phenyl)-3,4-dihydro-2H-isoquinolin-1-one (XI), 0.020 g (80% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683064B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-8024ddd2595540f89392f9b50d4deef3 |
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| Source note | uspto-grants-2010_03 |
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