Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479964Generated: October 28, 2026

Sodium borohydride → HCID 70929057, compound

https://huagongshe.com/reaction/1479964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67178105HCID 67178105—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 70929057HCID 70929057—

Reaction Steps

To (R)-4-(6-benzoyl-4,5-dimethyl-pyridazin-3-yl)-2-methyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-5′-carboxylic acid methyl ester (8 mg, 0.017 mmol) in MeOH (2 mL) is added sodium borohydride (170 μg, 0.004 mmol) in 15 minutes and the reaction mixture is stirred at room temperature for 1 h. The reaction mixture is diluted with DCM and washed with NaHCO3 and water. The organic solvent is separated and the solvent is removed under reduced pressure. Purification by HPLC of the crude product with acetonitril in water (from 10% to 100% with 3% 1-propanol) at 220 nm wavelength detection provides the desired product as off white powder. (6 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409871B2
Source datasetuspto-grants-2016_08
ORD IDord-3d67cf459b494c899bed2e3d85fc4a5d
Source noteuspto-grants-2016_08