Reaction equation
[Cl:1][C:2]1[C:3]([O:11][CH2:12][CH:13]2[CH2:15][CH2:14]2)=[CH:4][C:5]([C:8]([OH:10])=O)=[N:6][CH:7]=1.[NH2:16][C:17]([CH3:21])([CH3:20])[C:18]#[N:19]>>[C:18]([C:17]([NH:16][C:8]([C:5]1[CH:4]=[C:3]([O:11][CH2:12][CH:13]2[CH2:15][CH2:14]2)[C:2]([Cl:1])=[CH:7][N:6]=1)=[O:10])([CH3:21])[CH3:20])#[N:19]Participants
3
Procedure
The title compound was synthesized in analogy to Example 1, using 5-chloro-4-cyclopropylmethoxy-pyridine-2-carboxylic acid and 2-amino-2-methyl-propanenitrile (CAN 19355-69-2 as starting materials and isolated (50 mg, 78%) as colorless oil; LC-MS (UV peak area, m/z) 93.8%, 294.1001 (MH+).
Workup
- customisolated (50 mg, 78%) as colorless oil
Sources & evidence
- ORD record
- ord-116c0f1a1d25480890d20d308903682a
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409866B2
Linked notes
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