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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488008Generated: October 30, 2026

Sodium Hydroxide → HCID 178441450, compound

https://huagongshe.com/reaction/488008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant2-n-Butyl-1-{(5'-chloro-2'-cyanobiphenyl-4-yl)methyl]benzimidazoleHCID 22418003—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178441450HCID 178441450—

Reaction Steps

1.2 g of 2-n-butyl-1-{(5'-chloro-2'-cyanobiphenyl-4-yl)methyl}benzimidazole prepared in Preparation Example 8, 910 mg of sodium azide and 750 mg of ammonium chloride were heated while stirring in 50 ml of dimethylformamide as a reaction solvent at an internal temperature of 125° C. for 50 hr. After cooling, a dilute sodium hydroxide solution and ethyl acetate were added thereto for phase separation, thereby obtaining a watery phase. The watery phase was wealky acidified with acetic acid, extracted with chloroform and washed with water. The extract was dried over anhydrous magnesium sulfate, and the residue was subjected to silica gel chromatography (chloroform:etanol:acetic acid=98:2:0.2). A fraction of the intended title compound was concentrated and then recrystallized from ethyl acetate-isopropyl ethermethanol. The yield was 450 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298518
Source datasetuspto-grants-1994_03
ORD IDord-f80e9e377cea4632ae812343ec66b4b4
Source noteuspto-grants-1994_03