HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924321Generated: October 28, 2026
Sodium borohydride → HCID 57742987, compound
https://huagongshe.com/reaction/1924321
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57743086 | HCID 57743086 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57742987 | HCID 57742987 | 65% |
Reaction Steps
Methyl 6-bromo-3-(4-methoxybenzyl)-3H-imidazo[4,5-b]pyridine-7-carboxylate x210 (1.2 g, 3.19 mmol) is dissolved in absolute ethanol. NaBH4 (0.36 g, 3 eq, 9.57 mmol) is added at 5° C. under stirring. The cooling bath is removed after 4 h, and the reaction mixture is allowed to heat up to room temperature. The stirring is continued at this temperature for 20 h. The reaction mixture is evaporated in the vacuum of a rotary evaporator at 35° C., and the residue is partitioned in ethyl acetate/saturated aqueous NaHCO3 mixture. The organic layer is dried with anhydrous sodium sulfate and evaporated. The crude product is purified by chromatography on silicagel (dichloromethane/methanol) to afford 0.72 g of [6-bromo-3-(4-methoxybenzyl)-3H-imidazo[4,5-b]pyridin-7-yl]methanol x211.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178533B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-1714b3d3e1f24c01ab5296e11925c40f |
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| Source note | uspto-grants-2012_05 |
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