Sodium Hydroxide → 6-(5-(2-(4-Fluorobenzenesulphonylamino)ethyl)-N-methylpyrrol-2-yl)-6-(3-pyridyl)hexanoic acid

HRID 22109Notes

Reaction equation

HRID 22109 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH2:12][CH2:13][C:14]2[N:18]([CH3:19])[C:17]([C:20]([C:28]3[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=3)=[CH:21][CH2:22][CH2:23][CH2:24][C:25]([OH:27])=[O:26])=[CH:16][CH:15]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[OH-].[Na+].[H][H]>CO.[Pd]>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH2:12][CH2:13][C:14]2[N:18]([CH3:19])[C:17]([CH:20]([C:28]3[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=3)[CH2:21][CH2:22][CH2:23][CH2:24][C:25]([OH:27])=[O:26])=[CH:16][CH:15]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1

Participants

6

Procedure

A mixture of 2.36 g of 6-(5-(2-(4-fluorobenzenesulphonylamino)ethyl)-N-methyl-pyrrol-2-yl)-6-(3-pyridyl)hex-5-enoic acid, 0.4 g of sodium hydroxide and 1 g of 10% palladium/charcoal in 50 ml of methanol is hydrogenated under 5 bar of hydrogen pressure. Then the catalyst is filtered off, the filtrate is evaporated down, the residue is diluted with water, acidified and extracted with ethylene chloride. The organic extract is evaporated down and the residue recrystallised from ethyl acetate.

Workup

  1. filtrationThen the catalyst is filtered off
  2. customthe filtrate is evaporated down
  3. additionthe residue is diluted with water
  4. extractionextracted with ethylene chloride
  5. extractionThe organic extract
  6. customis evaporated down
  7. customthe residue recrystallised from ethyl acetate

Sources & evidence

ORD record
ord-196c63a240214338b610cf500a80de70
Source dataset
uspto-grants-1995_06
Patent number
US05426119

Reaction notes

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