HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1879112Erstellt: 25. Oktober 2026
Ethyl 2-(4-amino-2-fluorophenyl)acetate → Ethyl (4-{[(2-chloro-5-{[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}-2-fluorophenyl)acetate
https://huagongshe.com/reaction/1879112
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl 2-(4-amino-2-fluorophenyl)acetate | HCID 15840528 | — |
| Edukt | N-[2-(dimethylamino)ethyl]-N'-ethylcarbodiimide hydrochloride | HCID 57494384 | — |
| Edukt | 2-Chloro-5-{[(3-chlorophenyl)methyl]oxy}benzoic acid | HCID 59760049 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethyl (4-{[(2-chloro-5-{[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}-2-fluorophenyl)acetate | HCID 59163386 | 33% |
Reaktionsschritte
A solution of 2-chloro-5-{[(3-chlorophenyl)methyl]oxy}benzoic acid (207 mg, 0.7 mmol) in dichloromethane (3 ml) was treated with N-[2-(dimethylamino)ethyl]-N′-ethylcarbodiimide hydrochloride (201 mg, 1.05 mmol, 1.5 eq) and stirred at room temperature for 30 minutes. A solution of ethyl (4-amino-2-fluorophenyl)acetate (207 mg, 1.05 mmol, 1.5 eq) in dichloromethane (2 ml) was added and the resulting mixture heated at 40° C. overnight. On cooling, the mixture was diluted with methanol and purified by SCX cartridge eluting with methanol to afford the title compound as a yellow oil (110 mg). MS (ES+) m/z 476 [M+H]+ (C24H2035Cl2FNO4). 1H-NMR (400 MHz, d6-DMSO) δ 1.19 (3H, t, J 7.2), 3.68 (2H, s), 4.09 (2H, q, J 7.2), 5.20 (2H, s), 7.15-7.68 (10H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08314147B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-de727b0ead63478bb37214cd9fd71c6a |
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| Quellennotiz | uspto-grants-2012_11 |
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