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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287373Generated: November 1, 2026

Dansyl chloride → HCID 18704816, compound

https://huagongshe.com/reaction/2287373

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 0.05M 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 numberUS06083951
Source datasetuspto-grants-2000_07
ORD IDord-57356eb10e404759a4ceab0c75e83a84
Source noteuspto-grants-2000_07