1-Bromopropane → HCID 15342497, compound

HRID 341821Notes

Reaction equation

HRID 341821 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[C:16]3[C:11](=[CH:12][N:13]=[CH:14][CH:15]=3)[S:10][CH:9]=2)=[CH:3][CH:2]=1.[H-].[Na+].Br[CH2:20][CH2:21][CH3:22]>CN(C)C=O>[CH2:20]([N:7]([C:4]1[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=1)[C:8]1[C:16]2[C:11](=[CH:12][N:13]=[CH:14][CH:15]=2)[S:10][CH:9]=1)[CH2:21][CH3:22]

Participants

5

Procedure

3-(4-Pyridinylamino)thieno[2,3-c]pyridine (4 g) was added portionwise as a powder to a suspension of sodium hydride (60% oil dispersion, 0.8 g washed with heptane) in 50 mL of dimethylformamide. After anion formation was completed 1-bromopropane (2.2 g) was added. After stirring one hour the reaction mixture was poured into ice-water and extracted with ethyl acetate. The organic extract was washed with water saturated sodium chloride, and then was dried (anhydrous magnesium sulfate), filtered and evaporated to 5 g of a dark oil. Elution through silica with 5% methanol in ethyl acetate via flash column chromatography afforded 3.5 g of a yellow solid. Elution through alumina with ether via column chromatography afforded 2.8 g of a yellow solid. Recrystallization from heptane afforded 2.6 g (54.8%) of yellowish crystals, m.p. 119°-120° C.

Workup

  1. additionwas added
  2. extractionextracted with ethyl acetate
  3. extractionThe organic extract
  4. washwas washed with water saturated sodium chloride
  5. dry with materialwas dried (anhydrous magnesium sulfate)
  6. filtrationfiltered
  7. customevaporated to 5 g of a dark oil
  8. washElution through silica with 5% methanol in ethyl acetate via flash column chromatography

Sources & evidence

ORD record
ord-2e3e59b857784fe6b209aa3ea59d3355
Source dataset
uspto-grants-1999_01
Patent number
US05856335

Reaction notes

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