HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248122Erstellt: 26. Oktober 2026
1,2-Dichloroethane → 2,3-Dihydrothieno[3,2-b]quinolin-9-amine
https://huagongshe.com/reaction/248122
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Dihydro-3(2H)-thiophenone | HCID 61252 | — |
| Edukt | 2-Aminobenzonitrile | HCID 72913 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Produkt | 2,3-Dihydrothieno[3,2-b]quinolin-9-amine | HCID 14372828 | 31,8% |
Reaktionsschritte
Anthranilonitrile (4.80 g) and tetrahydrothiophen-3-one (8.17 g) were stirred until a homogeneous mixture was obtained and then freshly fused ZnCl2 (8.0 g) was added and the reaction mixture heated at 120°. After 2 hours, 30 ml of 1,2-dichloroethane was added and the reaction mixture refluxed for an additional 2 hours. At the end of this time the reaction mixture was distributed between 10% NaOH solution and 2-butanone, after which the organic phase was separated, dried, concentrated and purified by flash chromatography (5% i-PrOH/CH2Cl2). Combination of the product-containing fractions gave 2.61 g of product that was pure to thin layer chromatography. This product was combined with that obtained in another run and recrystallized from EtOAc to give analytically pure material, mp 210°-212°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05208330 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-95466a2915a543f5bae252fcc77eb8e9 |
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| Quellennotiz | uspto-grants-1993_05 |
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