HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7048Erstellt: 24. Oktober 2026
Ethylamine → cis-2-[(4-Chlorobenzenesulfonyl)-(4-ethylcarbamoyl-benzyl)-amino]-cycloheptanecarboxylic acid amide
https://huagongshe.com/de/reaction/7048
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethylamine | HCID 6341 | — |
| Edukt | cis-4-[[(2-Carbamoyl-cycloheptyl)-(4-chlorobenzenesulfonyl)-amino]-methyl]-benzoic acid methyl ester | HCID 11236936 | — |
| Produkt | cis-2-[(4-Chlorobenzenesulfonyl)-(4-ethylcarbamoyl-benzyl)-amino]-cycloheptanecarboxylic acid amide | HCID 69655987 | 18% |
Reaktionsschritte
cis-4-[[(2-Carbamoyl-cycloheptyl)-(4-chlorobenzenesulfonyl)-amino]-methyl]-benzoic acid methyl ester (50 mg, 0.10 mmol) and ethylamine (1.0 M in MeOH, 6 mL) were heated with stirring at 60° C. for 16 h. The solution was concentrated to dryness and the product purified by silica-gel column chromatography (20%–90% EtOAc/Hexanes) to afford 9.0 mg (18% yield) of the titled compound: 1 H NMR (DMSO-d6) δ 7.89 (m, 1 H), 7.80 (d, 2 H, J=8.0 Hz), 7.72 (d, 2 H, J=8.0 Hz), 7.64 (d, 2 H, J=8.0 Hz), 7.36 (d, 2 H, J=8.0 Hz), 7.32 (s br, 1 ), 6.67 (s br, 1 H), 4.58 (AB2,2 H,Δv=16,Jab=108 Hz), 3.97 (m, 1 H), 2.76 (m, 1 H), 2.26 (m, 2 H), 1.72 (m, 2 H), 1.35 (m, 8 H), 1.12 (t, 3 H, J=8.0 Hz); MS m/e 492.29 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07084178B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-075826d4fe38408cb9e4371c687d2ac0 |
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| Quellennotiz | uspto-grants-2006_08 |
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