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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467734Generated: October 30, 2026

Sodium borohydride → HCID 58548308, compound

https://huagongshe.com/reaction/467734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86660191HCID 86660191—
SolventEthanolHCID 702—
ProductHCID 58548308HCID 58548308—

Reaction Steps

To a stirred, cooled (0° C.) suspension of 6-acetyl-3-(pyrimidin-5-ylamino)-pyrazine-2-carboxylic acid (1-methyl-3-methylcarbamoyl-1H-pyrazol-4-yl)-amide (12 mg, 30.4 μmol) in ethanol (2 ml) under an argon atmosphere was added sodium borohydride (1.15 mg, 30.4 μmol) in one portion. Stirring was continued for 1 hr at rt. More sodium borohydride (3 eq.) was added in one portion. The mixture was heated to reflux and stirring as continued for 30 min. The reaction was cooled to rt and concentrated. The crude product was purified by silica gel chromatography using a CH2Cl2/MeOH gradient as eluent. The title compound (4 mg, 33%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623866B2
Source datasetuspto-grants-2014_01
ORD IDord-e00ebfb9982d45539402b93c0a8ac355
Source noteuspto-grants-2014_01