Cesium carbonate → (S)-4-((3-Bromopyridin-4-yl)methyl)-7-cyano-1,2,3,4-tetrahydrocyclopenta[b]indol-2-ylcarbamic acid isopropyl ester

HRID 449837Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 449837
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8]Cl.[CH:10]([O:13][C:14](=[O:30])[NH:15][C@@H:16]1[CH2:29][C:19]2[NH:20][C:21]3[CH:22]=[CH:23][C:24]([C:27]#[N:28])=[CH:25][C:26]=3[C:18]=2[CH2:17]1)([CH3:12])[CH3:11].C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C)C=O.C(OCC)(=O)C.ClCCl.O>[CH:10]([O:13][C:14](=[O:30])[NH:15][C@@H:16]1[CH2:29][C:19]2[N:20]([CH2:8][C:7]3[CH:6]=[CH:5][N:4]=[CH:3][C:2]=3[Br:1])[C:21]3[CH:22]=[CH:23][C:24]([C:27]#[N:28])=[CH:25][C:26]=3[C:18]=2[CH2:17]1)([CH3:12])[CH3:11]

Komponenten

8

Versuchsvorschrift

A mixture of 3-bromo-4-(chloromethyl)pyridine (3.16 g, 11.5 mmol), ((S)-7-cyano-1,2,3,4-tetrahydro-cyclopenta[b]indol-2-yl)-carbamic acid isopropyl ester (2.50 g, 8.82 mmol) and cesium carbonate (4.31 g, 13.2 mmol) in dimethylformamide (20 mL) is stirred at room temperature under nitrogen overnight. The reaction mixture is then diluted with ethyl acetate, dichloromethane, and water. The organic phase is separated, washed with water twice, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to obtain a brown oil (˜4.75 g). The oil is triturated with hexanes twice, then with ether twice. It is then purified by flash chromatography eluting with 30 to 60% ethyl acetate/hexanes to obtain an off-white solid (3.23 g, 81%). LC-ES/MS m/z (79Br/81Br) 453.0/455.0 [M+H]+.

Aufarbeitung

  1. customThe organic phase is separated
  2. washwashed with water twice
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-912c5da85ab34d98bd5e00be39c125d9
Quelldatensatz
uspto-grants-2013_07
Patentnummer
US08486943B2

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