Butyl bromide → 1-(4-Butoxyphenyl)cyclopropanecarboxylic Acid {4-[3-(acetylmethylamino)-pyrrolidin-1-yl]phenyl}amide
Reaction equation
[C:1]([CH2:4][NH:5][CH:6]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14]([NH:17][C:18]([C:20]3([C:23]4[CH:28]=[CH:27][C:26]([OH:29])=[CH:25][CH:24]=4)[CH2:22][CH2:21]3)=[O:19])=[CH:13][CH:12]=2)[CH2:7]1)(=[O:3])[CH3:2].[CH2:30](Br)[CH2:31][CH2:32][CH3:33]>>[C:1]([CH2:4][NH:5][CH:6]1[CH2:10][CH2:9][N:8]([C:11]2[CH:12]=[CH:13][C:14]([NH:17][C:18]([C:20]3([C:23]4[CH:28]=[CH:27][C:26]([O:29][CH2:30][CH2:31][CH2:32][CH3:33])=[CH:25][CH:24]=4)[CH2:21][CH2:22]3)=[O:19])=[CH:15][CH:16]=2)[CH2:7]1)(=[O:3])[CH3:2]Participants
3
Procedure
1-(4-Hydroxyphenyl)cyclopropanecarboxylic acid {4-[3-(acetylmethyl -amino)pyrrolidin-1yl]phenyl}amide was reacted with n-butyl bromide by method H. This resulted in the product with the molecular weight of 449.60 (C27H35N3O3); MS(ESI): 450 (M+H+).
Workup
- customThis resulted in the product with the molecular weight of 449.60 (C27H35N3O3)
Sources & evidence
- ORD record
- ord-bcfab6ff144d4240ac65e5fa4ab292ab
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07968550B2
Reaction notes
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