HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343360Generated: October 30, 2026
Dansyl chloride → HCID 18704816, compound
https://huagongshe.com/reaction/343360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dansyl chloride | HCID 11801 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18704816 | HCID 18704816 | 5.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861401 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-dd26de02f5674d088c44c6eea8a8497e |
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| Source note | uspto-grants-1999_01 |
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