2-Fluoro-4-isopropenyl-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide → HCID 16752625, compound

HRID 1260217Notes

Reaction equation

HRID 1260217 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([C:8]([CH3:10])=[CH2:9])[CH:5]=[CH:4][C:3]=1[S:11]([NH:14][C:15]1[CH:20]=[CH:19][C:18]([C@@H:21]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH3:28])[CH2:22]2)=[CH:17][CH:16]=1)(=[O:13])=[O:12]>CO.[Pd]>[F:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[S:11]([NH:14][C:15]1[CH:20]=[CH:19][C:18]([C@@H:21]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH3:28])[CH2:22]2)=[CH:17][CH:16]=1)(=[O:12])=[O:13]

Participants

4

Procedure

0.161 g of 2-fluoro-4-isopropenyl-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide (0.37 mmol) were dissolved in 20 ml methanol, a tip of a spatula 10% Pd/C added, and the reaction mixture hydrogenated for 3 h at 50° C. The reaction mixture was filtered over celite, washed with methanol, and the filtrate evaporated to dryness under reduced pressure. The residue was purified via silica gel chromatography on a chromabond column with ethyl acetate and ethyl acetate/methanol (10%). Fractions containing the product were combined, the solvent evaporated to yield 0.11 g of the title product.

Workup

  1. filtrationThe reaction mixture was filtered over celite
  2. washwashed with methanol
  3. customthe filtrate evaporated to dryness under reduced pressure
  4. customThe residue was purified via silica gel chromatography on a chromabond column with ethyl acetate and ethyl acetate/methanol (10%)
  5. additionFractions containing the product
  6. customthe solvent evaporated

Sources & evidence

ORD record
ord-f7536e984aa043e899a2c84a00b42327
Source dataset
uspto-grants-2013_06
Patent number
US08470810B2

Reaction notes

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