HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432279Erstellt: 24. Oktober 2026
4-(Trifluoromethyl)benzoyl chloride → HCID 178488213, Verbindung
https://huagongshe.com/de/reaction/432279
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Edukt | HCID 178488198 | HCID 178488198 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 178488213 | HCID 178488213 | 74% |
Reaktionsschritte
4-(Trifluoromethyl)-1-benzenecarbonyl chloride (262 mg, 1.256 mmol) in dichloromathane (1 mL) was added to a solution of trans-3-(4-amino-3-methoxyphenyl)-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (500 mg, 1.145 mmol) in pyridine (8 mL) at 0° C. After 30 minutes, the ice bath was removed the the reaction mixture was stirred at room temperature for 1.5 hour. Solvent was evaporated and the residue was purified by flash column chromatography using dichloromethane/methanol (80:20) as mobile phase to give trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-2-methoxyphenyl)-4-(trifluoromethyl)benzamide (516 mg, 74%). 1H NMR (CDCl3-d) δ 1.55 (m, 2H), 1.74 (m, 2H), 2.10-2.27 (m, 6H), 2.30 (s, 3H), 2.51 (m, 4H), 2.66 (m, 3H), 3.96 (s, 3H), 4.04 (s, 3H), 4.78 (m, 1H), 5.57 (bs, 2H), 7.30 (m, 2H), 7.79 (d, J=8.25 Hz, 2H), 8.04 (d, J=8.05 Hz, 2H), 8.38 (s, 1H), 8.64 (s, 1H), 8.68 (d, J=8.20 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06660744B1 |
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| Quelldatensatz | uspto-grants-2003_12 |
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| ORD ID | ord-674761fe84cf49cf87706657887bfec6 |
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| Quellennotiz | uspto-grants-2003_12 |
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