HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → 1-(Quinolin-6-yl)cyclopropan-1-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Boron trifluoride etherate | HCID 8000 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Quinoline-6-carbonitrile | HCID 592995 | — |
| Edukt | HCID 178418443 | HCID 178418443 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-(Quinolin-6-yl)cyclopropan-1-amine | HCID 63097228 | — |
Reaktionsschritte
Ethylmagnesium bromide (7.7 mmol, 3 M in ethyl ether) was added to a solution of quinoline-6-carbonitrile (0-4) (540 mg, 3.5 mmol) and Ti(Oi-Pr)4 (3.9 mmol, 1.16 mL) in Et2O (15 mL) at −70° C. The resulting yellow solution was stirred for 10 mins, warmed to room temperature over 1.5 h, and then was treated with BF3.OEt2 (7 mmol, 0.88 mL). The resulting mixture was stirred for 1 h. Then 1N aqueous HCl (11 mL) and ethyl ether (40 mL) were added, followed by NaOH (10% aq, 30 mL). The mixture was extracted with ethyl ether. The combined ethyl ether layers were dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to afford the crude title compound, which was used for the next step without further purification. MS (m/z): 185 (M+1)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08987269B2 |
| Quelldatensatz | uspto-grants-2015_03 |
| ORD ID | ord-b44d7f2fca014da9aa91f74bc59e9afa |
| Quellennotiz | uspto-grants-2015_03 |