HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 590076Erstellt: 24. Oktober 2026
N-(4-aminocyclohexyl)methanesulfonamide → HCID 178505151, Verbindung
https://huagongshe.com/de/reaction/590076
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-(4-aminocyclohexyl)methanesulfonamide | HCID 18348422 | — |
| Edukt | N-{3-[5-(2-Chloro-4-pyrimidinyl)-2-(1-pyrrolidinyl)-1,3-thiazol-4-yl]phenyl}-2,6-difluorobenzenesulfonamide | HCID 57989807 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | HCID 178505151 | HCID 178505151 | — |
Reaktionsschritte
N-{3-[5-(2-Chloro-4-pyrimidinyl)-2-(1-pyrrolidinyl)-1,3-thiazol-4-yl]phenyl}-2,6-difluorobenzenesulfonamide was dissolved in n-butanol and N-(4-aminocyclohexyl)methanesulfonamide (27.0 mg, 0.140 mmol) was added at rt followed by TEA (52.2 μl, 0.375 mmol). The reaction was heated to 60° C. for 12 h. Purified via Gilson Acidic HPLC (10 to 90% gradient, Acetonitrile/H2O+TFA; C18 column). Desired fractions were combined and washed with NaHCO3, dried over MgSO4 and solvent removed to give the title compound as a yellow solid (0.010 g). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.73 (d, J=5.1 Hz, 1H), 7.38-7.55 (m, 1H), 7.11-7.31 (m, 2H), 6.93-7.10 (m, 3H), 6.72-6.88 (m, 1H), 6.42-6.48 (m, 1H), 6.28-6.35 (m, 1H), 5.79-5.88 (m, 1H), 3.52-3.63 (m, 1H), 3.29-3.45 (m, 6H), 3.05-3.16 (m, 1H), 2.91 (s, 3H), 1.77-2.02 (m, 6H), 1.19-1.42 (m, 4H). MS (ESI): 690 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09233956B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-1a24509871d941f2b56521b58d7816d7 |
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| Quellennotiz | uspto-grants-2016_01 |
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