Ethylamine → 2-chloro-N-ethyl-5-nitropyridin-4-amine
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][N:3]=1.[CH2:12]([NH2:14])[CH3:13]>>[Cl:1][C:2]1[CH:7]=[C:6]([NH:14][CH2:12][CH3:13])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][N:3]=1Participants
3
Procedure
The title compound was prepared by the method of Example 1, Step 4 starting from the product of Example 1, Step 3 and ethylamine. MS (ES+) m/e 202 [M+H]+.
Sources & evidence
- ORD record
- ord-0dd130d9f5fe4c748a9e771248c2076e
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07547779B2
Reaction notes
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