Water → HCID 53824054, compound

HRID 648039Notes

Reaction equation

HRID 648039 reaction equation
[OH:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[H-].[Na+].[CH3:10][O:11][C:12]([C:14]1[S:18][C:17]2[CH:19]=[CH:20][C:21]([CH2:23]Br)=[CH:22][C:16]=2[CH:15]=1)=[O:13].O>CN(C)C=O>[CH3:10][O:11][C:12]([C:14]1[S:18][C:17]2[CH:19]=[CH:20][C:21]([CH2:23][O:1][C:2]3[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=3)=[CH:22][C:16]=2[CH:15]=1)=[O:13]

Participants

6

Procedure

3-Hydroxypyridine (0.40 g.) was dissolved in dry N,N-dimethylformamide (10 ml.) and sodium hydride (0.20 g. of 50% dispersion in mineral oil) was added portionwise with stirring and the resulting mixture was stirred at room temperature for 30 minutes. 5-(Bromomethyl)benzo[b]thiophene-2-carboxylic acid methyl ester (1.20 g.) in a few mls of dry N,N-dimethylformamide was then added and the mixture was stirred at room temperature for 30 minutes, and then poured into water. The mixture was extracted several times with ethyl acetate and the combined extracts were washed well with water and dried (Na2SO4). Evaporation of the solvent gave an oil which was chromatographed on silica gel. Elution with a mixture of chloroform and toluene (1:1) first gave mineral oil followed by pure product. Evaporation of the product-containing fractions gave a solid (0.40 g.) which was crystallized from isopropanol/petrol (b.p. 60°-80°) to give 5-(3-pyridyloxymethyl)benzo[b]thiophene-2-carboxylic acid methyl ester, m.p. 106°-107° C.

Workup

  1. stirringthe resulting mixture was stirred at room temperature for 30 minutes
  2. stirringthe mixture was stirred at room temperature for 30 minutes
  3. extractionThe mixture was extracted several times with ethyl acetate
  4. washthe combined extracts were washed well with water
  5. dry with materialdried (Na2SO4)
  6. customEvaporation of the solvent
  7. customgave an oil which
  8. customwas chromatographed on silica gel
  9. washElution
  10. additionwith a mixture of chloroform and toluene (1:1) first gave mineral oil
  11. customEvaporation of the product-containing fractions
  12. customgave a solid (0.40 g.) which
  13. customwas crystallized from isopropanol/petrol (b.p. 60°-80°)

Sources & evidence

ORD record
ord-461393f7c0384f92a9f5038f95af0f7b
Source dataset
uspto-grants-1983_10
Patent number
US04410539

Reaction notes

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