Allylamine → HCID 19791950, compound
Reaction equation
Cl[C:2]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH2:12]([NH2:15])[CH:13]=[CH2:14]>>[CH2:12]([NH:15][C:2]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1)[CH:13]=[CH2:14]Participants
3
Conditions
- Temperature
- 140 °C
Procedure
Methyl 2-chloropyridine-3-carboxylate (5 g) was reacted neat with allylamine (3.1 g) with heating at 140° C. for 4 hours. The volatiles were removed under reduced pressure and the residue chromatographed on silica gel eluting with ethyl acetate in hexane to afford 4.12 g of the title compound. MS (DCl/NH3) m/e 207 (M+H)+.
Workup
- customThe volatiles were removed under reduced pressure
- customthe residue chromatographed on silica gel eluting with ethyl acetate in hexane
Sources & evidence
- ORD record
- ord-2e88998d92db44b78485123dba46496a
- Source dataset
- uspto-grants-1993_10
- Patent number
- US05250548
Reaction notes
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