(2-methyl-1,3-thiazol-4-yl)acetic acid → HCID 59654967, compound
Reaction equation
[CH3:1][C:2]1[S:3][CH:4]=[C:5]([CH2:7][C:8]([OH:10])=O)[N:6]=1.[NH2:11][C:12]1[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][C:13]=1[C:20](=O)[C:21]1[CH:26]=[CH:25][C:24]([CH2:27][CH3:28])=[CH:23][CH:22]=1>>[CH2:27]([C:24]1[CH:23]=[CH:22][C:21]([C:20]2[C:13]3[C:12](=[CH:19][CH:18]=[C:15]([C:16]#[N:17])[CH:14]=3)[NH:11][C:8](=[O:10])[C:7]=2[C:5]2[N:6]=[C:2]([CH3:1])[S:3][CH:4]=2)=[CH:26][CH:25]=1)[CH3:28]Participants
3
Procedure
Synthesized from (2-methyl-thiazol-4-yl)-acetic acid and 4-Amino-3-(4-ethyl-benzoyl)-benzonitrile according to general procedure 2. Yield 27%.
Sources & evidence
- ORD record
- ord-a16002984d224c90808f1b673f95c257
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07326788B2
Reaction notes
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