HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411774Generated: October 27, 2026
Sodium cyanoborohydride → 5-Bromo-1-methyl-3-(6-(4-(oxetan-3-yl)piperazin-1-yl)pyridin-3-ylamino)pyrazin-2(1H)-one
https://huagongshe.com/reaction/1411774
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Reactant | 5-Bromo-1-methyl-3-(6-(piperazin-1-yl)pyridin-3-ylamino)-pyrazin-2(1H)-one | HCID 86684364 | — |
| Catalyst | ZINC;ethoxyethane;dichloride | HCID 162251561 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-1-methyl-3-(6-(4-(oxetan-3-yl)piperazin-1-yl)pyridin-3-ylamino)pyrazin-2(1H)-one | HCID 86684365 | 64% |
Reaction Steps
A mixture of 197d (0.75 g, 2.1 mmol), oxetan-3-one (0.24 mL, 4.2 mmol), NaBH3CN (0.32 g, 5.1 mmol), and zinc chloride/diethyl ether (5.1 mL, 5.1 mmol) in methanol (30 mL) was stirred at 50° C. for 5 hours. The solid was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with 10:1 dichloromethane/methanol to afford 197e (550 mg, 64%). MS-ESI: [M+H]+ 421.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921353B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-16edb30ff4a045928a50f32fbcb9e870 |
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| Source note | uspto-grants-2014_12 |
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