1-Bromopropane → HCID 15342497, compound
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- additionwas added
- extractionextracted with ethyl acetate
- extractionThe organic extract
- washwas washed with water saturated sodium chloride
- dry with materialwas dried (anhydrous magnesium sulfate)
- filtrationfiltered
- customevaporated to 5 g of a dark oil
- 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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