HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Acid → 4-Chloro-5-[3-(tert-butyldimethylsiloxy)propyloxy]-7-[1-(tert-butoxycarbonyl)-5-(dimethylaminomethyl)indol-2-yl]isoindolinone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| Edukt | 4-Chloro-5-[3-(tert-butyldimethylsiloxy)propoxy]-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone | HCID 86628331 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-Chloro-5-[3-(tert-butyldimethylsiloxy)propyloxy]-7-[1-(tert-butoxycarbonyl)-5-(dimethylaminomethyl)indol-2-yl]isoindolinone | HCID 68490993 | 83% |
Reaktionsschritte
In a similar manner to Step 2 of Example 6, 4-chloro-5-[3-(tert-butyldimethylsiloxy)propoxy]-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone (74.9 mg, 0.125 mmol) was dissolved in acetonitrile (2.5 mL), and the solution was treated with 2.0 mol/L dimethylamine-THF solution (0.63 mL, 1.25 mmol), acetic acid (0.072 mL, 1.25 mmol) and sodium triacetoxyborohydride (76.5 mg, 0.375 mmol), followed by purification by flash column chromatography (chloroform/methanol=19/1, 4/1) to obtain 4-chloro-5-[3-(tert-butyldimethylsiloxy)propyloxy]-7-[1-(tert-butoxycarbonyl)-5-(dimethylaminomethyl)indol-2-yl]isoindolinone (65.0 mg, yield 83%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07745641B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-2511e98e75604dafa94df0a2bce4c564 |
| Quellennotiz | uspto-grants-2010_06 |