Methanesulfonic Acid → (2-{3-[1-(5-Fluoro-pyridin-2-yl)-vinyl]-benzo[b]thiophen-2-yl}-ethyl)-dimethyl-amine

HRID 746611Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 746611
[CH3:1][N:2]([CH3:24])[CH2:3][CH2:4][C:5]1[S:9][C:8]2[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=2[C:6]=1[C:14]([C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][N:18]=1)(O)[CH3:15].CS(O)(=O)=O.[NH4+].[OH-]>C(Cl)Cl>[F:23][C:20]1[CH:21]=[CH:22][C:17]([C:14]([C:6]2[C:7]3[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=3[S:9][C:5]=2[CH2:4][CH2:3][N:2]([CH3:1])[CH3:24])=[CH2:15])=[N:18][CH:19]=1

Komponenten

5

Versuchsvorschrift

To a solution of 1-[2-(2-dimethylamino-ethyl)-benzo[b]thiophen-3-yl]-1-(5-fluoro-pyridin-2-yl)-ethanol in (1.65 g, 4.79 mmol) in methylene chloride (30 mL) at room temperature, methanesulfonic acid (310 uL, 4.8 mol) was added dropwise and the reaction was allowed to stir for 2 hours. Additional methanesulfonic acid (3.1 mL, 47.9 mmol) was added and the reaction was stirred for 2 more hours. The reaction was neutralized with aq NH4OH and was extracted with methylene chloride. Organic layer was concentrated. The reaction mixture was chromatographed on silica gel with 9:1 DCM:MeOH as eluent to afford 923 mg of (2-{3-[1-(5-fluoro-pyridin-2-yl)-vinyl]-benzo[b]thiophen-2-yl}-ethyl)-dimethyl-amine (Compound 7-2) (59%).

Aufarbeitung

  1. stirringthe reaction was stirred for 2 more hours
  2. extractionwas extracted with methylene chloride
  3. concentrationOrganic layer was concentrated
  4. customThe reaction mixture was chromatographed on silica gel with 9:1 DCM

Quellen und Nachweise

ORD-Eintrag
ord-706b3f1ab12142ec846fb90f6e0df641
Quelldatensatz
uspto-grants-2008_07
Patentnummer
US07393865B2

Notizen zur Reaktion

Wird geladen…