HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 423959Erstellt: 24. Oktober 2026
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- → HCID 178513610, Verbindung
https://huagongshe.com/de/reaction/423959
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- | HCID 77857 | — |
| Edukt | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Edukt | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Edukt | Cyano-2-(ethylamino)benzoic acid | HCID 66674956 | — |
| Edukt | HCID 178464543 | HCID 178464543 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 178513610 | HCID 178513610 | — |
Reaktionsschritte
Part D: (S)-4-(2-(1-(1-(4-Cyano-2-(ethylamino)phenyl)vinylamino)-2-phenylethyl)-1H-imidazol-4-yl)benzamide: Cyano-2-(ethylamino)benzoic acid from Example 140 Part C (40 mg, 0.2 mmol), Bop reagent (108 mg, 0.24 mmol), and Et3N (0.28 mL) were added together with 5 mL of THF. The mixture was stirred at RT for 15 minutes and (S)-4-(2-(1-Amino-2-phenylethyl)-1H-imidazol-4-yl)benzamide (107 mg, 0.2 mmol), obtained from N-boc-(L)-phenylalanine and 4-(2-Bromo-acetyl)-benzonitrile by the sequential application of the procedures described for Example 1 Part A, Example 28 Part A and Example 1 Part B, was added. The resulting mixture was heated to reflux under N2 for 2 h. The solvent were removed. The residue was dissolved in EtOAc and washed with water and brine. It was dried over MgSO4, concentrated, and purified by ISCO flash chromatography (silica, EtOAc/hexane) to give 50 mg of the desired product. LC/MS: 479.3 (M+1)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08101778B2 |
|---|
| Quelldatensatz | uspto-grants-2012_01 |
|---|
| ORD ID | ord-0a96e639c63c4dcb9f7a0d394d39577a |
|---|
| Quellennotiz | uspto-grants-2012_01 |
|---|