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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169772Generated: November 1, 2026

Sodium borohydride → HCID 89876292, compound

https://huagongshe.com/reaction/2169772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 89876303HCID 89876303—
SolventEthanolHCID 702—
ProductHCID 89876292HCID 8987629275.2%

Reaction Steps

To a stirred solution of 6-acetyl-4-(2,3-dichloroindol-1-yl)-5-methoxy-2-methyl-pyridazin-3-one (500 mg, 1.37 mmol) in ethanol (1 mL) at 0° C. is added sodium borohydride (79 mg, 2.05 mmol). After stirring for 20 min, the reaction is quenched with water (10 mL), then concentrated under reduced pressure to remove most of the ethanol. The aqueous solution is then extracted with Et2O (20 mL×2), then concentrated under reduced pressure to give the desired product 4-(2,3-dichloroindol-1-yl)-6-(1-hydroxyethyl)-5-methoxy-2-methyl-pyridazin-3-one (379 mg, 1.03 mmol, 75%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09049864B2
Source datasetuspto-grants-2015_06
ORD IDord-4bdf3cb1509349539fb7f9fe5c0e1d02
Source noteuspto-grants-2015_06