HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500943Generated: November 2, 2026
Sodium borohydride → HCID 178504854, compound
https://huagongshe.com/reaction/1500943
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178472512 | HCID 178472512 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178504854 | HCID 178504854 | 21.2% |
Reaction Steps
To a solution of ethyl trans-3-(5-chloro-2-{[3-(methylsulfonyl)-1H-pyrazolo[3,4-c]pyridin-1-yl]methyl}-1H-benzimidazol-1-yl)cyclobutanecarboxylate (80 mg, 0.16 mmol) in EtOH was added NaBH4 (80 mg, 2.1 mmol) in portions at RT. The mixture was then heated at 60° C. for 1 hour. The reaction was completed as indicated by LC/MS. The mixture was quenched with 1N HCl to pH7. After the solvent was removed by concentration, the residue was purified by preparative-HPLC to afford 15.1 mg of [trans-3-(5-chloro-2-{[3-(methylsulfonyl)-1H-pyrazolo[3,4-c]pyridin-1-yl]methyl}-1H-benzimidazol-1-yl)cyclobutyl]methanol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206191B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-a410aded39d94beba158f26ce61f1814 |
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| Source note | uspto-grants-2015_12 |
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