Methyl 2-Chloro-6-methylisonicotinate → HCID 67510693, compound
Reaction equation
Cl[C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH3:12])[N:11]=1)[C:5]([O:7][CH3:8])=[O:6].[CH:13]1([CH2:16][C:17]([NH2:19])=[O:18])[CH2:15][CH2:14]1>>[CH:13]1([CH2:16][C:17]([NH:19][C:2]2[CH:3]=[C:4]([CH:9]=[C:10]([CH3:12])[N:11]=2)[C:5]([O:7][CH3:8])=[O:6])=[O:18])[CH2:15][CH2:14]1Participants
3
Procedure
The title compound is prepared in 67% yield (316 mg) from methyl 2-chloro-6-methylisonicotinate (350 mg, 1.89 mmol) and 2-cyclopropylacetamide (243 mg, 2.45 mmol) by the similar manner in Step-1 of Carboxylic acid-4.
Sources & evidence
- ORD record
- ord-80dfb664aa9a4eee8e2c2f43f745b20f
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09302991B2
Reaction notes
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