Hydrochloric Acid → 1-Cyclohexyl-3-[2,4-dichloro-4'-(3-dimethylamino-propoxy)-biphenyl-3-ylmethyl]-pyrrolidin-2-one hydrochloride

HRID 2235322Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2235322
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([Cl:28])=[C:10]([C:24]([Cl:27])=[CH:25][CH:26]=2)[CH2:11][CH:12]2[CH2:16][CH2:15][N:14]([CH:17]3[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]3)[C:13]2=[O:23])=[CH:4][CH:3]=1.[I-].[Na+].C(=O)([O-])[O-].[Cs+].[Cs+].Cl.Br[CH2:39][CH2:40][CH2:41][N:42]([CH3:44])[CH3:43].Cl>CC(C)=O.C(Cl)Cl.CCOCC>[ClH:27].[CH:17]1([N:14]2[CH2:15][CH2:16][CH:12]([CH2:11][C:10]3[C:9]([Cl:28])=[C:8]([C:5]4[CH:6]=[CH:7][C:2]([O:1][CH2:39][CH2:40][CH2:41][N:42]([CH3:44])[CH3:43])=[CH:3][CH:4]=4)[CH:26]=[CH:25][C:24]=3[Cl:27])[C:13]2=[O:23])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]1

Komponenten

9

Versuchsvorschrift

Place 3-(3-(4-hydroxyphenyl)-2,6-dichlorobenzyl)-1-cyclohexylpyrrolidin-2-one (0.200 g, 0.478 mmol), sodium iodide (0.072 g, 0.478 mmol, and cesium carbonate (1.25 g, 3.82 mmol) in acetone (lOmL). Add 3-bromo-N,N-dimethylpropan-1-amine hydrochloride (0.194 g, 0.956 mmol) and stir at room temperature for 3 hours. Add water and extract with DCM. Dry, filter, and concentrate. Purify by silica gel to give the free base. Dissolve in DCM and add 2M HCl in ether. Concentrate to give 84 mg (33%) of the title compound as a tan solid. Mass spectrum (apci) m/z=503.3 (M+H).

Aufarbeitung

  1. extractionAdd water and extract with DCM
  2. customDry
  3. filtrationfilter
  4. concentrationconcentrate
  5. customPurify by silica gel
  6. customto give the free base
  7. concentrationConcentrate

Quellen und Nachweise

ORD-Eintrag
ord-5b70c7b2402747c89b2d1b7cd14da646
Quelldatensatz
uspto-grants-2010_05
Patentnummer
US07713979B2

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