Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | 2-Chloro-5-nitrobenzenesulfonamide | HCID 66784 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2-Benzylamino-5-nitro-benzenesulfonamide | HCID 24858397 | 83,4% |
Reaktionsschritte
A solution of 2-chloro-5-nitro-benzenesulfonamide (20 g, 84.52 mmol) in acetonitrile (169 mL) was treated with benzylamine (13.85 mL, 126.78 mmol), diisopropyl ethylamine (29.44 mL, 169.04 mmol) and stirred for 16 h at 55° C. The reaction was cooled to 25° C., poured into water (1.0 L) then placed in an ice bath while stirring. After 4 h a precipitate was filtered off and washed with the mother liquor to afford the desired product, 2-benzylamino-5-nitro-benzenesulfonamide (21.65 g, 70.45 mmol, 83.3%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ: 4.64 (2H, d, J=4.6 Hz), 6.81 (1H, d, J=9.4 Hz), 7.23-7.44 (6H, m), 7.77 (2H, bs), 8.11 (1H, dd, J1=9.4 Hz, J2=2.3 Hz), 8.49 (1H, d, J=3.1 Hz). LC-MS (ESI) calcd for C13H13N3O4S 307.06, found 308.2 [M+H+] (100%), 615.2 [2M+H+] (81%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07582626B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-7471437e19c74501b00ff0a0c15570ab |
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| Quellennotiz | uspto-grants-2009_09 |
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