Pyridine → HCID 54043483, Verbindung

HRID 1079240Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1079240
[CH3:1][N:2]1[C@H:11]2[C@@:6]([CH3:23])([C:7]3[CH:15]=[CH:14][C:13]([C:16]4[CH:21]=[CH:20][CH:19]=[C:18]([NH2:22])[CH:17]=4)=[CH:12][C:8]=3[CH2:9][CH2:10]2)[CH2:5][CH2:4][C:3]1=[O:24].N1C=CC=CC=1.ClCCl.[C:34](Cl)(=[O:39])[C:35]([CH3:38])([CH3:37])[CH3:36]>C(Cl)(Cl)Cl>[CH3:1][N:2]1[C@H:11]2[C@@:6]([CH3:23])([C:7]3[CH:15]=[CH:14][C:13]([C:16]4[CH:21]=[CH:20][CH:19]=[C:18]([NH:22][C:34](=[O:39])[C:35]([CH3:38])([CH3:37])[CH3:36])[CH:17]=4)=[CH:12][C:8]=3[CH2:9][CH2:10]2)[CH2:5][CH2:4][C:3]1=[O:24]

Komponenten

6

Versuchsvorschrift

A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-8-(3-aminophenyl)-10b-methyl 1,2,3,4,4a,-5,6,10b-octahydrobenzo[f]quinolin-3-one (31 mg, 0,097 mmol), N,N-dimethylaminopyridine (3 mg, 0,024 mmol), 1 mL of pyridine and 0.5 mL of dichloromethane. The solution was cooled to 0°, and excess pivaloyl chloride (0,086 mL, 0.69 mmol) was added. The stirred mixture was allowed to warm to room temperature over 2 h. The mixture was diluted with chloroform, and washed with 5% aqueous hydrochloric acid solution, water, 5% queous sodium hydroxide solution, water, and the combined organic extracts were dried over sodium sulfate, concentrated and chromatographed on silica gel (ethyl acetate eluent) to give 25 mg (64%) of the title compound as a yellow solid. mp 95°-98°. FDMS m/e=404. α[D]589 =+62.50 (c=0.16, chloroform).

Aufarbeitung

  1. temperatureThe solution was cooled to 0°
  2. washwashed with 5% aqueous hydrochloric acid solution, water, 5% queous sodium hydroxide solution, water
  3. dry with materialthe combined organic extracts were dried over sodium sulfate
  4. concentrationconcentrated
  5. customchromatographed on silica gel (ethyl acetate eluent)

Quellen und Nachweise

ORD-Eintrag
ord-23eb63c02f18465c9bd39eb3d10edd5a
Quelldatensatz
uspto-grants-1996_08
Patentnummer
US05550134

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