HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343372Generated: October 26, 2026
Hydrochloric Acid → 5-dimethylamino-N-(5-bromo-6-chloro-2-pyrazinyl)-1-naphthalenesulphonamide
https://huagongshe.com/reaction/343372
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dansyl chloride | HCID 11801 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-6-chloropyrazin-2-amine | HCID 18180207 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 5-dimethylamino-N-(5-bromo-6-chloro-2-pyrazinyl)-1-naphthalenesulphonamide | HCID 18704780 | 52.1% |
Reaction Steps
2-Amino-5-bromo-6-chloropyrazine (0.417 g) was added to a stirred suspension of sodium hydride (oil-free; 0.24 g) in dry dimethoxyethane (20 ml). When evolution of hydrogen ceased, 5-dimethylamino-1-naphthalenesulphonyl chloride (0.594 g) was added. The mixture was stirred for 24 hours and then water (25 ml) and 2M hydrochloric acid (2 ml) were added. The mixture was extracted with ethyl acetate (2×25 ml) and the extracts were dried (MgSO4). Volatile material was removed by evaporation and the residue was purified by elution with ethyl acetate/hexane (1:3 v/v) through a silica gel Mega Bond Elut column to give 5-dimethylamino-N-(5-bromo-6-chloro-2-pyrazinyl)-1-naphthalenesulphonamide (0.46 g), m.p. 180°-182° C. (after trituration with ether); mass spectrum (+ve FAB, methanol/NBA): 442 (M+).
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-f17097e3066a42538a61eb286182a9b2 |
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| Source note | uspto-grants-1999_01 |
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