Bromomethylcyclopropane → HCID 24965855, compound
Reaction equation
[CH2:1]([C:5]1[NH:6][C:7](=[O:18])[N:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[O:16][CH3:17])[CH:9]=1)[CH:2]([CH3:4])[CH3:3].Br[CH2:20][CH:21]1[CH2:23][CH2:22]1>>[CH:21]1([CH2:20][N:6]2[C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])=[CH:9][N:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[O:16][CH3:17])[C:7]2=[O:18])[CH2:23][CH2:22]1Participants
3
Procedure
This material was obtained in analogy to the procedure outlined in example 23 from 4-isobutyl-1-(2-methoxy-phenyl)-1,3-dihydro-imidazol-2-one (obtained in example 42, 150 mg) by alkylation with bromomethylcyclopropane (90 mg). 3-Cyclopropylmethyl-4-isobutyl-1-(2-methoxy-phenyl)-1,3-dihydro-imidazol-2-one was obtained as a colorless oil (52 mg). MS (ESI): 301.2 (MH+).
Workup
- customThis material was obtained in analogy to the procedure
Sources & evidence
- ORD record
- ord-8b79cbe8bebd43bca8487be3e8295dac
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08129423B2
Reaction notes
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