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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881989Generated: November 3, 2026

Sodium triacetoxyborohydride → HCID 59331327, compound

https://huagongshe.com/reaction/1881989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-[(3S)-3-Methyl-1-piperazinyl]ethanoneHCID 11435008—
Reactant6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehydeHCID 59331419—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
ProductHCID 59331327HCID 5933132772.3%

Reaction Steps

To a solution of 6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehyde (200 mg) in 1,2-dichloroethane (3 mL) was added (3S)-1-acetyl-3-methylpiperazine (140 mg), and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added sodium triacetoxyborohydride (273 mg), and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried (MgSO4) and concentrated. The residue was subjected to basic silica gel column chromatography, and the title compound (184 mg, yield 72%) was obtained as a colorless amorphous solid from a fraction eluted with ethyl acetate. MS: 591 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-5e89cd320dbb4d3ca95ba498960bf77c
Source noteuspto-grants-2012_11