Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706776Generated: October 30, 2026

Hydrazine → HCID 178434382, compound

https://huagongshe.com/reaction/706776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantN-[4-(5-acetyl-6-chloro-pyrazin-2-yl)-phenyl]-2,3-dichloro-benzenesulfonamideHCID 86678949—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 178434382HCID 178434382—

Reaction Conditions

Temperature120 °C

Reaction Steps

N-[4-(5-acetyl-6-chloro-pyrazin-2-yl)-phenyl]-2,3-dichloro-benzenesulfonamide (230 mg) was suspended in a mixture of 2 ml iPrOH and 2 ml 35% hydrazine in water at RT and heated to 120° C. by microwave irradiation (Biotage Initiator™ apparatus) for 20 min under stirring in a sealed vessel. The reaction mixture was left to cool to RT, quenched with a saturated aqueous sodium bicarbonate solution (10 ml) and extracted with EtOAc (3×30 ml). The combined organic phases were dried over sodium sulfate, filtered and evaporated to afford the crude product. Purification by recrystallisation from an acetone-water mixture afforded the title compound as a pale yellow solid after drying under vacuum. Yield: 81.6 mg (38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174993B2
Source datasetuspto-grants-2015_11
ORD IDord-8d2b471f888443baa4e50695afcf7393
Source noteuspto-grants-2015_11