HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721455Erstellt: 25. Oktober 2026
Triethylamine → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-(3-diethylaminopropyl)thiourea
https://huagongshe.com/reaction/721455
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Thiophosgene | HCID 10040 | — |
| Edukt | 4-(6,7-Dimethoxyquinazolin-4-yloxy)aniline | HCID 11616363 | — |
| Edukt | (2-Aminopropyl)diethylamine | HCID 16643481 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-(3-diethylaminopropyl)thiourea | HCID 21889988 | 12% |
Reaktionsschritte
4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (50 mg) was dissolved in N,N-dimethylformamide (2 ml) and triethylamine (1 ml) to prepare a solution. Thiophosgene (50 mg) was then added to the solution, and the mixture was stirred at room temperature for 6 hr. Next, N,N-diethylpropylenediamine (50 mg) was added thereto, and the mixture was further stirred at room temperature for 15 hr. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated brine in that order. The organic layer was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by HPLC using chloroform/methanol for development to give the title compound (10 mg, yield 12%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07135466B2 |
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| Quelldatensatz | uspto-grants-2006_11 |
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| ORD ID | ord-f6751be79ae04707bf0e40138e54490e |
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| Quellennotiz | uspto-grants-2006_11 |
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