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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693745Generated: November 1, 2026

Sodium borohydride → HCID 57537637, compound

https://huagongshe.com/reaction/1693745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57537502HCID 57537502—
SolventMethanolHCID 887—
ProductHCID 57537637HCID 5753763757.1%

Reaction Steps

Sodium borohydride (85.5 mg, 2.25 mmol) was added to methanol (5 mL) at 0° C. After 5 min, 2-(2-amino-5-bromo-pyridin-3-yl)-N,N-dimethyl-2-oxo-acetamide (408 mg, 1.50 mmol) in MeOH (15 mL) was added. After 1 h, the reaction was quenched by addition of saturated NH4Cl and the mixture was concentrated in vacuo. The residue was extracted with ethyl acetate, dried over Na2SO4 and purified by silica gel chromatography using DCM and MeOH to afford 2-(2-amino-5-bromo-pyridin-3-yl)-2-hydroxy-N,N-dimethyl-acetamide (234 mg, 57.1%) as a brown oily solid. The material was used in the next step. MS: m/z 274 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158647B2
Source datasetuspto-grants-2012_04
ORD IDord-cbc77870c1844edaa56693d68e85566f
Source noteuspto-grants-2012_04