Potassium Carbonate → HCID 18999619, compound

HRID 2260400Notes

Reaction equation

HRID 2260400 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:4][CH:3]=1.[C:13]([O-])([O-])=O.[K+].[K+].Br[CH:20]1[CH2:24][CH2:23][CH2:22][CH:21]1[NH:25][S:26]([C:29]1[CH:34]=[CH:33][C:32]([Cl:35])=[CH:31][CH:30]=1)(=[O:28])=[O:27]>CN(C=O)C>[Cl:35][C:32]1[CH:33]=[CH:34][C:29]([S:26]([NH:25][CH:21]2[CH2:22][CH2:23][CH2:24][CH:20]2[O:1][C:2]2[CH:3]=[CH:4][C:5]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:6][CH:7]=2)(=[O:28])=[O:27])=[CH:30][CH:31]=1

Participants

5

Conditions

Temperature
80 °C

Procedure

A mixture of 2.5 g (15 mmoles) of methyl 4-hydroxybenzeneacetate, 4 g (30 mmoles) of K2CO3 and 30 ml of DMF is heated to 80° C. A solution of 5 g (14.8 mmoles) of N-(2-bromocyclopentyl)-4-chlorobenzenesulfonamide as in example 5a is added dropwise thereto, in 50 ml of DMF. The mixture is stirred 5 h at 80° C. After cooling, the solid which is present is filtered and rinsed with ethyl acetate. The filtrate which is diluted with water is extracted with ethyl acetate. The organic phase is washed with water, dried over Na2SO4 and concentrated under reduced pressure. The residue which is purified by chromatography on a column of silica (eluant: hexane-ethyl acetate 1/1) gives 6.2 g (yield=99.5%) of a yellow liquid.

Workup

  1. temperatureAfter cooling
  2. filtrationthe solid which is present is filtered
  3. washrinsed with ethyl acetate
  4. additionThe filtrate which is diluted with water
  5. extractionis extracted with ethyl acetate
  6. washThe organic phase is washed with water
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customThe residue which is purified by chromatography on a column of silica (eluant: hexane-ethyl acetate 1/1)

Sources & evidence

ORD record
ord-f1b6dd6703a243e5ba583c97ae36dd5d
Source dataset
uspto-grants-1995_12
Patent number
US05476846

Reaction notes

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