Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formic Acid | HCID 284 | — |
| Edukt | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Edukt | 2-Amino-6-bromonaphthalene | HCID 348404 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 2-Bromo-6-(sulfamoylamino)naphthalene | HCID 22559043 | — |
Reaktionsschritte
A solution of chlorosulfonyl isocyanate (870 μl, WAKO) in benzene (10 ml) was added dropwise with formic acid (377 μl, WAKO) under ice cooling, warmed to room temperature, stirred for 19.5 hours, then heated to 40° C. and further stirred for 4 hours. The reaction mixture was added dropwise with a solution (5 ml) of 2-amino-6-bromonaphthalene (443 mg) in benzene under ice cooling, warmed to room temperature and stirred for 21.5 hours. The reaction mixture was filtered, and the obtained solid was added with ethyl acetate and mixed. The mixture was filtered again, and then the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1) to obtain the title compound (Intermediate 28, 158 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06867320B2 |
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| Quelldatensatz | uspto-grants-2005_03 |
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| ORD ID | ord-a3cb2ca8d20d416a9157656051eb274a |
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| Quellennotiz | uspto-grants-2005_03 |
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