HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2390712Erstellt: 24. Oktober 2026
Quinoline → N-(4-{4-amino-7-[(1Z)-3-(diethylamino)prop-1-enyl]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide
https://huagongshe.com/de/reaction/2390712
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Quinoline | HCID 7047 | — |
| Edukt | N-(4-{4-amino-7-[3-(diethylamino)prop-1-ynyl]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide | HCID 18451160 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Lindlars catalyst | HCID 131709914 | — |
| Lösungsmittel | Pyridine ethanol | HCID 21975839 | — |
| Produkt | N-(4-{4-amino-7-[(1Z)-3-(diethylamino)prop-1-enyl]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide | HCID 44432309 | 38% |
Reaktionsschritte
A solution of N-(4-{4-amino-7-[3-(diethylamino)prop-1-ynyl]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide (0.135 g, 0.251 mmol) in ethanol/pyridine (15 mL/10 mL) was treated with Lindlar's catalyst (0.027 g), quinoline (0.05 g, 0.38 mmol), and hydrogen (55 psi) in a Parr Hydrogenator. The reaction mixture was shaken for 1H. The catalyst was filtered through celite. The solvent was removed under reduced pressure. The crude material was purified by preparative HPLC to afford 0.051 g (38%) of the title compound. 1H NMR (DMSO-d6, 400 MHz) δ 9.50 (s, 1H), 8.00-7.98 (d, 1H), 7.81 (s, 1H), 7.71-7.69 (d, 1H), 7.60-7.57 (m, 2H), 7.35-7.33 (m, 2H), 7.21-7.21 (m, 1H), 7.17-7.13 (t, H), 7.10-7.08 (d, 1H), 6.56-6.53 (d, 1H), 5.90-5.88 (dt, 1H), 5.60 (brs, 2H), 4.04 (s, 3H), 3.91 (s, 3H), 3.30-3.28 (m, 2H), 2.49-2.44 (q, 4H), 0.93-0.89 (t, 6H); LCMS (conditions a) Rt 3.28 min (95%), MH+ 540.3.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08273736B2 |
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| Quelldatensatz | uspto-grants-2012_09 |
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| ORD ID | ord-dee40f65bce140c1953a898170b940a6 |
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| Quellennotiz | uspto-grants-2012_09 |
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