HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 415136Erstellt: 25. Oktober 2026
Water → Benzyl 4-(4-carbamoylbenzo[d]oxazol-2-yl)benzyl(methyl)carbamate
https://huagongshe.com/reaction/415136
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 2-(4-(((Benzyloxycarbonyl)(methyl)amino)methyl)phenyl)benzo[d]oxazole-4-carboxylic acid | HCID 66620558 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Benzyl 4-(4-carbamoylbenzo[d]oxazol-2-yl)benzyl(methyl)carbamate | HCID 66621310 | — |
Reaktionsschritte
Oxalyl chloride (218 mg, 1.72 mmol) is slowly added to a solution of 2-(4-(((benzyloxycarbonyl)(methyl)-amino)methyl)phenyl)benzo[d]oxazole-4-carboxylic acid (0.65 g, 1.57 mmol) in dichloromethane (10 mL) with stirring. The reaction mixture is warmed to 50° C. for 4 h and then cooled to 25° C. The solution is condensed in vacuum and then slowly added to 28% NH4OH (6 mL). The mixture is warmed to 50° C. and stirred for another 2 h. Water (50 mL) is added to the reaction mixture and the slurry is cooled to 25° C. The product is filtered and the cake is washed with water, dried to afford benzyl 4-(4-carbamoylbenzo[d]oxazol-2-yl)benzyl(methyl)carbamate solid. MS (ESI) m/e 416 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08088760B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-b42b0d50f7e2420886cb5161335fddd1 |
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| Quellennotiz | uspto-grants-2012_01 |
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