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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343360Generated: October 30, 2026

Dansyl chloride → HCID 18704816, compound

https://huagongshe.com/reaction/343360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDansyl chlorideHCID 11801—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-3,5-dibromopyrazineHCID 620004—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 18704816HCID 187048165.3%

Reaction Conditions

Temperature95 °C

Reaction Steps

Sodium hydride (60% dispersion in oil; 0.16 g) was added to a solution of 2-amino-3,5-dibromopyrazine (0.506 g) in N,N-dimethylformamide (30 ml). When evolution of hydrogen ceased, 5-dimethylamino-1-naphthalenesulphonyl chloride (0.54 g) was added and the solution was heated at 95° C. for 18 hours. Volatile material was removed by evaporation and water (50 ml) was added to the residue. The mixture was extracted with ethyl acetate (20 ml), and the aqueous layer was neutralised with 0.05H aqueous acetic acid (40 ml) and extracted with ethyl acetate (3×25 ml). The extracts were washed with water (20 ml) and saturated sodium chloride solution (20 ml) and dried (MgSO4). Volatile material was removed by evaporation and the residue was purified by elution with dichloromethane through a silica gel Mega Bond Elut column. The resulting foam was triturated with ether/hexane (1:1 v/v) to give 5-(dimethylamino)-N-(3,5-dibromo-2-pyrazinyl)-1-naphthalenesulphonamide (0.052 g), m.p. 178° C.; mass spectrum (+ve FAB, methanol/NBA): 485 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861401
Source datasetuspto-grants-1999_01
ORD IDord-dd26de02f5674d088c44c6eea8a8497e
Source noteuspto-grants-1999_01