6-Isopropoxy-2-methylamino-3-nitropyridine → 6-Isopropoxy-N2-methylpyridine-2,3-diamine
Reaction equation
[CH:1]([O:4][C:5]1[N:10]=[C:9]([NH:11][CH3:12])[C:8]([N+:13]([O-])=O)=[CH:7][CH:6]=1)([CH3:3])[CH3:2]>CO.[Pd]>[NH2:13][C:8]1[C:9]([NH:11][CH3:12])=[N:10][C:5]([O:4][CH:1]([CH3:2])[CH3:3])=[CH:6][CH:7]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A procedure similar to that described in Example 6 was repeated, except that 2.38 9 of 6-isopropoxy-2-methylamino-3-nitropyridine (prepared as described in Preparation 100) were hydrogenated in 50 ml of methanol in the presence of 0.50 g of 10 % w/w palladium-on-charcoal. After working up the product as described in Example 6, 2.00 g of the title compound having Rf=0.62 (on silica gel thin layer chromatography using ethyl acetate as the developing solvent) were obtained.
Sources & evidence
- ORD record
- ord-3fb265161a44410798552df37db1ad64
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05739345
Reaction notes
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