HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzyl chloroformate → benzyl N-(4-chloro-3-nitrophenyl)carbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | 4-Chloro-3-nitroaniline | HCID 12477 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | benzyl N-(4-chloro-3-nitrophenyl)carbamate | HCID 4935650 | — |
Reaktionsschritte
In one example, 4-chloro-3-nitroaniline reacted with CbzCl in dichloromethane in the presence of diisopropylethylamine. The product benzyl 4-chloro-3-nitrophenylcarbamate was isolated following flash chromatography. Following procedures in Examples 12, 13, and 15, final product benzyl 1-(2-acetamidoethyl)-3-(4-methoxyphenyl)-2-oxo-1,2-dihydroquinoxalin-6-ylcarbamate was isolated following reverse-phase HPLC with C(18) column eluting with water and acetonitrile. The product of the reaction, benzyl 1-(2-acetamidoethyl)-3-(4-methoxyphenyl)-2-oxo-1,2-dihydroquinoxalin-6-ylcarbamate, is a compound of formula I in which R1 is —CH2CH2NHAc, R2 is benzyloxycarbonyl, R3 is 4-methoxyphenyl.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07893066B2 |
| Quelldatensatz | uspto-grants-2011_02 |
| ORD ID | ord-1aa8b452bd6044edbec9610814f5d3e2 |
| Quellennotiz | uspto-grants-2011_02 |