Triethylamine → (E)-3-(4-{(S)-1-[2-(2-methyl-1H-indol-3-yl)-acetyl]-pyrrolidin-2-yl}-phenyl)-acrylic acid methyl ester
Reaktionsgleichung
Cl.[CH3:2][O:3][C:4](=[O:18])/[CH:5]=[CH:6]/[C:7]1[CH:12]=[CH:11][C:10]([C@@H:13]2[CH2:17][CH2:16][CH2:15][NH:14]2)=[CH:9][CH:8]=1.C(N(CC)CC)C.Cl.C(N=C=NCCCN(C)C)C.ON1C2C=CC=CC=2N=N1.[CH3:48][C:49]1[NH:50][C:51]2[C:56]([C:57]=1[CH2:58][C:59](O)=[O:60])=[CH:55][CH:54]=[CH:53][CH:52]=2>CN(C)C=O.ClCCl>[CH3:2][O:3][C:4](=[O:18])/[CH:5]=[CH:6]/[C:7]1[CH:12]=[CH:11][C:10]([C@@H:13]2[CH2:17][CH2:16][CH2:15][N:14]2[C:59](=[O:60])[CH2:58][C:57]2[C:56]3[C:51](=[CH:52][CH:53]=[CH:54][CH:55]=3)[NH:50][C:49]=2[CH3:48])=[CH:9][CH:8]=1Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a stirred solution of (E)-3-((S)-4-pyrrolidin-2-yl-phenyl)-acrylic acid methyl ester hydrochloride (0.3 g, 1.12 mmol) in N,N-dimethylformamide (20 mL) was added sequentially triethylamine (0.5 mL, 3.58 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.24 g, 1.25 mmol), 1-hydroxybenzotriazole (0.17 g, 1.25 mmol) and 2-methylindole-3-acetic acid (0.235 g, 1.24 mmol). The reaction was stirred for 16 h and diluted with dichloromethane, and the solution was washed with a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (2% methanol in dichloromethane) to obtain (E)-3-(4-{(S)-1-[2-(2-methyl-1H-indol-3-yl)-acetyl]-pyrrolidin-2-yl}-phenyl)-acrylic acid methyl ester as a colorless oil (0.42 g, 1.03 mmol, 93% yield).
Aufarbeitung
- washthe solution was washed with a saturated aqueous solution of sodium chloride
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe crude product was purified by silica gel column chromatography (2% methanol in dichloromethane)
Quellen und Nachweise
- ORD-Eintrag
- ord-a8076f69a55742b5aa81ac0dc76d7c6b
- Quelldatensatz
- uspto-grants-2013_01
- Patentnummer
- US08349883B2
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