HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Aminobenzyl alcohol → HCID 57474716, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Aminobenzyl alcohol | HCID 21439 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | HCID 57474573 | HCID 57474573 | — |
| Edukt | HCID 57474717 | HCID 57474717 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 57474716 | HCID 57474716 | 86% |
Reaktionsschritte
Ethyl 5-nitro-2-(2-(hydroxymethyl)phenylamino)-6-(2-methoxyphenylamino)pyrimidine-4-carboxylate. Ethyl 2-chloro-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylate (See Example 30.A) (0.300 g, 0.852 mmol), 2-aminobenzyl alcohol (0.125 g, 1.2 mmol) and diisopropylethylamine (0.296 g) were reacted according to General Procedure C, except at room temperature and in dimethylformamide (5 ml). The crude reaction mixture was condensed and purified using Biotage chromatography (60 to 100% EtOAc in hexanes) to afford the title compound (0.323 g, 86%). MS (ESI) m/z 440.5 [M+1]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08383634B2 |
| Quelldatensatz | uspto-grants-2013_02 |
| ORD ID | ord-0f74feac840e4890ab527f36cd025e46 |
| Quellennotiz | uspto-grants-2013_02 |