5-Iodo-2-(3-methyloxetan-3-yl)-1H-imidazole-4-carbonitrile → Methyl 3-(4-cyano-2-(3-methyloxetan-3-yl)-1H-imidazol-5-yl)-4-methylbenzoate
Reaction equation
CC1NC([C:8]2[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=2[CH3:18])[C:11]([O:13][CH3:14])=[O:12])=C(C)N=1.I[C:20]1[NH:24][C:23]([C:25]2([CH3:29])[CH2:28][O:27][CH2:26]2)=[N:22][C:21]=1[C:30]#[N:31].IC1NC(C)=NC=1C>>[C:30]([C:21]1[N:22]=[C:23]([C:25]2([CH3:29])[CH2:28][O:27][CH2:26]2)[NH:24][C:20]=1[C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=1[CH3:18])[C:11]([O:13][CH3:14])=[O:12])#[N:31]Participants
4
Procedure
The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 5.6, except 5-iodo-2-(3-methyloxetan-3-yl)-1H-imidazole-4-carbonitrile (compound 202.3) was used in place of 5-iodo-2,4-dimethyl-1H-imidazole (compound 5.5). m/z (ES+) 312 (M+H)+.
Sources & evidence
- ORD record
- ord-31234d1eed85436e828f49d1492923b9
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09428502B2
Reaction notes
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