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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178120Generated: October 30, 2026

Ammonium Chloride → HCID 117653151, compound

https://huagongshe.com/reaction/2178120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant3-Cyano-4-fluorobenzenesulfonyl chlorideHCID 2778908—
ReactantHCID 63362875HCID 63362875—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117653151HCID 11765315136%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a suspension of N-(2,4-dimethoxybenzyl)pyridazin-3-amine (Preparation 19, 1.0 g, 4.00 mmol) in THF (15 mL) at −20° C. was slowly added LiHMDS (1M, 4.0 mL, 4.00 mmol). The reaction mixture was left to stir at −20° C. for 30 minutes and then cooled to −78° C. To the reaction mixture was slowly added 3-cyano-4-fluorobenzene-1-sulfonyl chloride (0.8 g, 3.64 mmol) suspended in THF (15 mL). The reaction mixture was slowly warmed to room temperature and left at room temperature for 18 hours. To the vessel was added saturated aqueous NH4Cl solution (30 mL) and the product was extracted with EtOAc (25 mL). The organic layer was washed with saturated brine (40 mL), dried over MgSO4, and the solvent removed under vacuum. The residue was purified using silica gel column chromatography eluting with 70% EtOAc in heptanes to afford the title compound as an orange oil (561 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067922B2
Source datasetuspto-grants-2015_06
ORD IDord-ff9016a948c945e49b01aeddd44a0276
Source noteuspto-grants-2015_06