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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693736Generated: November 1, 2026

Sodium borohydride → HCID 57537679, compound

https://huagongshe.com/reaction/1693736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57537624HCID 57537624—
SolventMethanolHCID 887—
ProductHCID 57537679HCID 5753767972.82%

Reaction Steps

A solution of {3-[4-chloro-3-(2-fluoro-phenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-phenyl}-oxazol-2-yl-methanone (22 mg, 0.040 mmol) in MeOH (0.25 mL) was added to a cold suspension (0° C.) of NaBH4 (1.59 mg, 0.042 mmol) in MeOH (0.25 mL). After 1 h, the mixture was quenched by addition of saturated ammonium chloride and the solution was concentrated to a solid. The residue was triturated with ethyl acetate to afford {3-[4-chloro-3-(2-fluoro-phenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-phenyl}-oxazol-2-yl-methanol (16 mg, 72.82%). MS: m/z 550 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158647B2
Source datasetuspto-grants-2012_04
ORD IDord-27d0f130bbf743bda156ba6fea3ff744
Source noteuspto-grants-2012_04