Ethylenediamine → N~1~-(Pyridin-2-yl)ethane-1,2-diamine
Reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[NH2:8][CH2:9][CH2:10][NH2:11]>>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:8][CH2:9][CH2:10][NH2:11]Participants
3
Procedure
2-Bromopyridine (10.00 g, 63.3 mmol) was added dropwise to 1,2-diaminoethane (76.00 g, 126.6 mmol) under nitrogen at 20° C. with stirring. The reaction mixture was stirred at 20° C. for 4 h. and then under reflux for 24 h. The reaction mixture was concentrated in vacuo and purified by column chromatography on flash silica eluting with dichloromethane, ethanol and ammonia (30:8:1) to afford the title compound as a red oil (1.23 g). TLC SiO2, (Dichloromethane, ethanol, ammonia; 30:8:1) Rf=0.14 Mass Spectrum m/z 138 (MH+ for C7H11N3).
Workup
- stirringThe reaction mixture was stirred at 20° C. for 4 h.
- temperatureunder reflux for 24 h
- concentrationThe reaction mixture was concentrated in vacuo
- custompurified by column chromatography on flash silica eluting with dichloromethane, ethanol and ammonia (30:8:1)
Sources & evidence
- ORD record
- ord-6924697d956a4d269cb4a0e942a68ef3
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06610665B1
Reaction notes
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