HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 641783Erstellt: 25. Oktober 2026
5-Chloro-1,3-benzodioxol-4-amine → N-(5-chloro-1,3-benzodioxol-4-yl)-5-morpholin-4-yl-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine
https://huagongshe.com/reaction/641783
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-Chloro-1,3-benzodioxol-4-amine | HCID 11367253 | — |
| Edukt | 4-Chloro-5-morpholino-7-(2-pyrrolidin-1-ylethoxy)quinazoline | HCID 22140709 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | N-(5-chloro-1,3-benzodioxol-4-yl)-5-morpholin-4-yl-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine | HCID 11974116 | 9,4% |
Reaktionsschritte
A mixture of 4-chloro-5-morpholino-7-(2-pyrrolidin-1-ylethoxy)quinazoline (0.27 g), 6-chloro-2,3-methylenedioxyaniline (0.14 g) and isopropanol (4 ml) was stirred and heated to 80° C. for 1 hour. The mixture was evaporated and the residue was dissolved in a 49:1 mixture of methylene chloride and a saturated methanolic ammonia solution. The mixture was filtered and the filtrate was poured onto a column of silica and eluted with a 97:3 mixture of methylene chloride and a saturated methanolic ammonia solution. The material so obtained was triturated under diethyl ether. The resultant solid was isolated, washed with diethyl ether and dried under vacuum. There was thus obtained the title compound (0.035 g); NMR Spectrum: (CDCl3) 1.85 (br s, 4H), 2.65 (br s, 4H), 3.0 (m, 2H), 3.08 (m, 2H), 3.18 (d, 2H), 3.82 (m, 2H), 4.05 (m, 2H), 4.25 (m, 2H), 6.05 (s, 2H), 6.75 (d, 1H), 6.95-7.1 (m, 3H), 8.52 (s, 1H); Mass Spectrum: M+H+ 498 and 500.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07696214B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-f20da184c2cb463fb3d623f89b56b373 |
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| Quellennotiz | uspto-grants-2010_04 |
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