6-(Trifluoromethyl)pyridine-2-carboxylic acid → HCID 86620721, compound
Reaction equation
[C:1]([C:3]1[C:4]([C:20]([F:23])([F:22])[F:21])=[C:5]2[C:9](=[CH:10][CH:11]=1)[N:8]([CH2:12][C:13](=[NH:16])[NH:14][OH:15])[C:7]([CH:17]1[CH2:19][CH2:18]1)=[CH:6]2)#[N:2].[F:24][C:25]([F:36])([F:35])[C:26]1[N:31]=[C:30]([C:32](O)=O)[CH:29]=[CH:28][CH:27]=1>>[CH:17]1([C:7]2[N:8]([CH2:12][C:13]3[N:16]=[C:32]([C:30]4[CH:29]=[CH:28][CH:27]=[C:26]([C:25]([F:35])([F:24])[F:36])[N:31]=4)[O:15][N:14]=3)[C:9]3[C:5]([CH:6]=2)=[C:4]([C:20]([F:22])([F:23])[F:21])[C:3]([C:1]#[N:2])=[CH:11][CH:10]=3)[CH2:19][CH2:18]1Participants
3
Procedure
Synthesized as described in Example 72 from 2-[5-cyano-2-cyclopropyl-4-(trifluoromethyl)-1H-indol-1-yl]-N-hydroxyethanimidamide (Example 364B) and 6-(trifluoromethyl)-2-pyridinecarboxylic acid: MS (ES) m/z 478 (M+1).
Workup
- customSynthesized
Sources & evidence
- ORD record
- ord-2811fd18bd4f4409b1aaccadff11dd96
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07572820B2
Reaction notes
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