1,2-Dichloroethane → tert-butyl (R)-1-((3S,4S)-4-(4-chlorophenyl)-3,4-dihydroxy-3-methylpiperidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamate

HRID 238347Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 238347
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@:8]2([OH:16])[CH2:13][CH2:12][NH:11][CH2:10][C@:9]2([CH3:15])[OH:14])=[CH:4][CH:3]=1.[C:17]([NH:24][C@@H:25]([C:29](O)=[O:30])[CH:26]([CH3:28])[CH3:27])([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18].C1C=CC2N(O)N=NC=2C=1.C(Cl)CCl.CCN(C(C)C)C(C)C>C(Cl)Cl.CN(C=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@:8]2([OH:16])[CH2:13][CH2:12][N:11]([C:29](=[O:30])[C@H:25]([NH:24][C:17](=[O:18])[O:19][C:20]([CH3:23])([CH3:22])[CH3:21])[CH:26]([CH3:28])[CH3:27])[CH2:10][C@@:9]2([OH:14])[CH3:15])=[CH:4][CH:3]=1

Komponenten

8

Versuchsvorschrift

To a mixture of (3S,4S)-4-(4-chlorophenyl)-3-methylpiperidine-3,4-diol (91 g, 376 mmol), Boc-D-Valine (83.1 g, 382 mmol), HOBt (69.2 g, 452 mmol), EDC (87 g, 452 mmol) in CH2Cl2 (800 mL) and DMF (80 mL) was added DIPEA (132 mL, 753 mmol) at room temperature. The mixture was stirred at room temperature overnight. The reaction was concentrated and the residue partitioned between EtOAc and water. The EtOAc layer was washed with 1N HCl, sat. aq. NaHCO3, and brine to give the crude product (180 g, ˜80% purity) which was used directly in the next transformation.

Aufarbeitung

  1. concentrationThe reaction was concentrated
  2. customthe residue partitioned between EtOAc and water
  3. washThe EtOAc layer was washed with 1N HCl, sat. aq. NaHCO3, and brine

Quellen und Nachweise

ORD-Eintrag
ord-78d2ad7d84b148b0b02fb1bae43c42c0
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08642622B2

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