Acetic acid, azido-, ethyl ester → Ethyl[4-(6-chloro-2-methylpyridin-3-yl)-1h-1,2,3-triazol-1-yl]acetate
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([C:9]#[CH:10])=[CH:4][CH:3]=1.[CH2:11]([O:13][C:14](=[O:19])[CH2:15][N:16]=[N+:17]=[N-:18])[CH3:12]>>[CH2:11]([O:13][C:14](=[O:19])[CH2:15][N:16]1[CH:10]=[C:9]([C:5]2[C:6]([CH3:8])=[N:7][C:2]([Cl:1])=[CH:3][CH:4]=2)[N:18]=[N:17]1)[CH3:12]Participants
3
Procedure
The title compound was prepared as described in Example 413, Step 2 using 6-chloro-3-ethynyl-2-methylpyridine (250 mg, 1.65 mmol) and ethylazidoacetate (0.93 ml, 1.65 mmol) as starting materials
Sources & evidence
- ORD record
- ord-0c31978d95e04f518bcadce7d4da3ce4
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367706B2
Reaction notes
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