Potassium Carbonate → HCID 59401866, compound

HRID 1916906Notes

Reaction equation

HRID 1916906 reaction equation
Cl.[CH3:2][CH:3]1[CH2:7][CH2:6][CH2:5][N:4]1[CH:8]1[CH2:12][CH2:11][NH:10][CH2:9]1.F[C:14]1[CH:15]=[CH:16][C:17]([N+:21]([O-:23])=[O:22])=[C:18]([CH3:20])[CH:19]=1.C(=O)([O-])[O-].[K+].[K+]>CS(C)=O>[CH3:2][CH:3]1[CH2:7][CH2:6][CH2:5][N:4]1[CH:8]1[CH2:12][CH2:11][N:10]([C:14]2[CH:15]=[CH:16][C:17]([N+:21]([O-:23])=[O:22])=[C:18]([CH3:20])[CH:19]=2)[CH2:9]1

Participants

5

Conditions

Temperature
85 °C

Procedure

2-Methyl-[1,3′]bipyrrolidinyl hydrochloride (Intermediate (ii) obtained above, 5.3 g, 21.6 mmol, 1.12 equiv.) was dissolved in anhydrous DMSO (30 mL). To this solution was added 5-fluoro-2-nitrotoluene (3.00 g, 18.78 mmol, 1 equiv.), followed by powdered potassium carbonate (8.9 g, 65 mmol). The suspension was heated on an oil bath to 85° C. for 4 h when the starting material was consumed as determined by TLC (5% MeOH in DCM) and LC/MS. To the suspension were added 20 mL of water and 50 mL of DCM. The two layers were separated, and the aqueous layer was extracted with DCM (20 mL×2). The combined DCM extracts were washed with sodium bicarbonate (20 mL), and brine (15 mL×2), dried (anhydrous potassium carbonate), filtered, and concentrated in vacuo. The crude product was purified on a silica gel column, eluted with 5% MeOH in DCM to get the title compound as a yellow solid after drying, 5.47 g (100%). MS: 290 (M+H+).

Workup

  1. customwas consumed
  2. additionTo the suspension were added 20 mL of water and 50 mL of DCM
  3. customThe two layers were separated
  4. extractionthe aqueous layer was extracted with DCM (20 mL×2)
  5. washThe combined DCM extracts were washed with sodium bicarbonate (20 mL), and brine (15 mL×2)
  6. dry with materialdried (anhydrous potassium carbonate)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe crude product was purified on a silica gel column
  10. washeluted with 5% MeOH in DCM

Sources & evidence

ORD record
ord-1565f43f903f461e82cf46946ec685f0
Source dataset
uspto-grants-2013_12
Patent number
US08618159B2

Reaction notes

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