1-Hydroxybenzotriazole → (2S)-2-{(1R,2S)-2-[2-(3-hydroxy-phenyl)-ethylcarbamoyl]-1-methylsulfanyl-propyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
Reaktionsgleichung
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][C@H:9]1[C@H:13]([S:19][CH3:20])[C@H:14]([C:16]([OH:18])=O)[CH3:15])=[O:7])([CH3:4])([CH3:3])[CH3:2].Br.[OH:22][C:23]1[CH:24]=[C:25]([CH:29]=[CH:30][CH:31]=1)[CH2:26][CH2:27][NH2:28].F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.C1C=CC2N(O)N=NC=2C=1.C(N(C(C)C)CC)(C)C>C(Cl)Cl>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][C@H:9]1[C@H:13]([S:19][CH3:20])[C@H:14]([C:16](=[O:18])[NH:28][CH2:27][CH2:26][C:25]1[CH:29]=[CH:30][CH:31]=[C:23]([OH:22])[CH:24]=1)[CH3:15])=[O:7])([CH3:2])([CH3:3])[CH3:4]Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of (2S)-2-[(1R,2S)-2-carboxy-1-methylsulfanyl-propyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (1.7 g, 5.6 mmol) in CH2Cl2 (20 mL) were added 3-hydroxyphenethylamine hydrobromide (2.44 g, 11.2 mmol), BOP(3.72 g, 8.4 mmol), HOBT (1.29 g, 8.4 mmol), and diisopropylethylamine (4.88 mL, 28.0 mmol) at room temperature. After being stirred at room temperature for 2 hr, the mixture was quenched with 1N HCl (80 mL×3), extracted with AcOEt, dried (MgSO4) and concentrated in vacuo to give a crude oil, which was purified by flash column chromatography (hexane:AcOEt=1:1) to give (2S)-2-{(1R,2S)-2-[2-(3-hydroxy-phenyl)-ethylcarbamoyl]-1-methylsulfanyl-propyl}-pyrrolidine-1-carboxylic acid tert-butyl ester as a gum (2.07 g, 87%).
Aufarbeitung
- customthe mixture was quenched with 1N HCl (80 mL×3)
- extractionextracted with AcOEt
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto give a crude oil, which
- customwas purified by flash column chromatography (hexane:AcOEt=1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-843db06507cd4bf590471b7a274ebb05
- Quelldatensatz
- uspto-grants-2004_05
- Patentnummer
- US06737409B2
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