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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925552Generated: October 28, 2026

Sodium borohydride → HCID 59487296, compound

https://huagongshe.com/reaction/1925552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 67521469HCID 67521469—
SolventEthanolHCID 702—
ProductHCID 59487296HCID 5948729691.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

70 mg (1.8 mmol) of NaBH4 were added in portions at 0° C. to a solution of 350 mg (0.9 mmol) of N-(3,3-dimethyl-2-oxo-butyl)-2-[3-(4-fluoro-phenyl)-propylsulfanyl]-pyridine-3-carboxylic acid amide (exemplary compound 125) in EtOH (7 ml). Stirring was then carried out for 2 h at RT. The mixture was then cooled to 0° C., quenched with a sat. aq. NH4Cl sol. (20 ml) and concentrated in vacuo. The residue was taken up in EA and the solution was washed with a 1M aq. NaHCO3 sol., water and brine, dried over Na2SO4, filtered and concentrated in vacuo. CC (hexane/EA 3:2) of the residue yielded 320 mg (0.82 mmol, 91%) of 2-[3-(4-fluorophenyl)-propylsulfanyl]-N-(2-hydroxy-3,3-dimethyl-butyl)-pyridine-3-carboxylic acid amide. MS: m/z 391.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178684B2
Source datasetuspto-grants-2012_05
ORD IDord-e26675737c4d49f6a7952eecab47658d
Source noteuspto-grants-2012_05