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HRID 480269Erstellt: 25. Oktober 2026
N,N,N',N'-Tetramethylazodicarboxamide → 2-(2-(4-(4-(3-(tert-butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic Acid Methyl Ester
https://huagongshe.com/reaction/480269
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N,N',N'-Tetramethylazodicarboxamide | HCID 4278 | — |
| Edukt | Tributylphosphine | HCID 13831 | — |
| Edukt | tert-Butyl (3-(hydroxymethyl)phenyl)carbamate | HCID 14523557 | — |
| Edukt | Methyl 2-(4-(4-hydroxyphenoxy)phenylacetamido)benzoate | HCID 20602792 | — |
| Lösungsmittel | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Produkt | 2-(2-(4-(4-(3-(tert-butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic Acid Methyl Ester | HCID 20602791 | 83% |
Reaktionsschritte
2-(2-(4-(4-Hydroxyphenoxy)phenyl)acetylamino)benzoic acid methyl ester obtained by the Reference Example 24 (315 mg, 0.83 mmol) was dissolved in 20 ml of methylene chloride-THF mixture (1:1 v/v), added with 3-(tert-butoxycarbonylamino)benzyl alcohol (465 mg, 2.1 mmol), 1,1′-azobis(N,N′-dimethylformamide) (359 mg, 2.08 mmol) and tri-n-butyl phosphine (520 ml, 2.1 mmol) and the reaction mixture was stirred over a night. After completing the reaction, the solvent was removed under reduced pressure and the obtained crude residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate 75:25 v/v) to obtain the subject compound (404 mg, 0.693 mmol) in the form of a colorless gummy substance. The result of 1H-NMR was consistent with the above structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06649656B1 |
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| Quelldatensatz | uspto-grants-2003_11 |
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| ORD ID | ord-c8aa473702e94ae9a3d2f401d66fb394 |
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| Quellennotiz | uspto-grants-2003_11 |
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