5-Ethynyl-1-methyl-1H-imidazole → N-[2-(3-Methyl-3H-imidazol-4-ylethynyl)-benzyloxy]-2-[(pyridin-4-ylmethyl)-amino]-benzamide
Reaction equation
I[C:2]1[CH:26]=[CH:25][CH:24]=[CH:23][C:3]=1[CH2:4][O:5][NH:6][C:7](=[O:22])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][CH2:15][C:16]1[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=1.[C:27]([C:29]1[N:33]([CH3:34])[CH:32]=[N:31][CH:30]=1)#[CH:28]>>[CH3:34][N:33]1[C:29]([C:27]#[C:28][C:2]2[CH:26]=[CH:25][CH:24]=[CH:23][C:3]=2[CH2:4][O:5][NH:6][C:7](=[O:22])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[NH:14][CH2:15][C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)=[CH:30][N:31]=[CH:32]1Participants
3
Procedure
Starring materials: N-(2-Iodo-benzyloxy)-2-[(pyridin-4-ylmethyl)-amino]-benzamide (see Example 360) and 5-ethynyl-1-methyl-1-H-imidazole (Aldrich).
Sources & evidence
- ORD record
- ord-56b14976577647638fccbbae62e1d431
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08034811B2
Reaction notes
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