HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925552Generated: October 28, 2026
Sodium borohydride → HCID 59487296, compound
https://huagongshe.com/reaction/1925552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 67521469 | HCID 67521469 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59487296 | HCID 59487296 | 91.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08178684B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-e26675737c4d49f6a7952eecab47658d |
|---|
| Source note | uspto-grants-2012_05 |
|---|