HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3,4-Dichlorobenzyl chloride → HCID 66924343, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride | HCID 66924378 | — |
| Produkt | HCID 66924343 | HCID 66924343 | 73% |
Reaktionsschritte
A mixture of 2-fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride (240 mg; 0.89 mmol) (Example 126, Step 3) was heated with 3,4-dichlorobenzyl chloride (0.15 mL; 2.0 mmol) and triethylamine (0.3 mL; 2.0 mmol) to 50° C. for 16 hours. Reaction was cooled and quenched with dilute HCl and mixture extracted with ethyl acetate (2×20 mL). Combined organics washed with water, saturated sodium bicarbonate, brine and dried over Na2SO4. Crude material was purified by chromatography using 0.5-2% methanol/DCM gradient to afford 2-[1-(3,4-dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile as a yellow oil. (280 mg; 73% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09067897B2 |
| Quelldatensatz | uspto-grants-2015_06 |
| ORD ID | ord-9575f5bd241f4c0abc2c5beb1af07039 |
| Quellennotiz | uspto-grants-2015_06 |