HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 985077Erstellt: 25. Oktober 2026
Ethyl Acetate → ((2-bromo)acetyl]amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane
https://huagongshe.com/reaction/985077
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Bromoacetyl bromide | HCID 61147 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane | HCID 22508955 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | ((2-bromo)acetyl]amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane | HCID 86759616 | — |
Reaktionsschritte
To a stirring solution of 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane (7.51 g, 21.369 mmoles) in anhydrous tetrahydrofuran (100 ml) under a nitrogen atmosphere at 0° C. was added diisopropylethylamine (4.1 ml, 23.537 mmoles) and bromoacetyl bromide (2.05 ml, 23.530 mmoles). After 2 hours, ethyl acetate was added and the reaction mixture washed with water twice, 1.0 N hydrochloric acid (2×), saturated sodium bicarbonate solution (2×), and brine. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to a tan foam on a rotary evaporator. In this manner the 2-[((2-bromo)acetyl]amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane was obtained in quantitative yield. No further purification was necessary.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06869957B1 |
|---|
| Quelldatensatz | uspto-grants-2005_03 |
|---|
| ORD ID | ord-6ff406f4bdca4dbf871362fe986d9cdb |
|---|
| Quellennotiz | uspto-grants-2005_03 |
|---|