HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → Tert-butyl (6-chloro-4-iodopyridin-3-yl)(methyl)carbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | tert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamate | HCID 53415320 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Tert-butyl (6-chloro-4-iodopyridin-3-yl)(methyl)carbamate | HCID 57443399 | 99,4% |
Reaktionsschritte
To the solution of tert-butyl(6-chloro-4-iodopyridin-3-yl)carbamate (61 g, 0.172 mol) in 300 mL of anhydrous THF was added 60% NaH (7.6 g, 0.189 mol) at 0° C. under N2 atmosphere. After the addition was finished, the solution was stirred for 30 min, and then the solution of MeI (26.92 g, 0.189 mol) in 100 mL of dry THF was added. Then the solution was stirred at 0° C. for 3 hrs. TLC indicated the reaction was over. Water was added for quench, and EtOAc was added to extract twice. The combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to afford 63 g of crude tert-butyl(6-chloro-4-iodopyridin-3-yl)(methyl)carbamate used into the following de-protection without the further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09403772B2 |
| Quelldatensatz | uspto-grants-2016_08 |
| ORD ID | ord-31e8b106c3e24af6b1f1325304239bce |
| Quellennotiz | uspto-grants-2016_08 |