Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 49832941, compound
Reaction equation
[CH3:1][N:2]1[C:10]([CH2:11][N:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)=[N:9][C:8]2[C:3]1=[N:4][C:5]([N:24]1[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=3[N:26]=[C:25]1[CH3:33])=[N:6][C:7]=2[N:18]1[CH2:23][CH2:22][O:21][CH2:20][CH2:19]1.Br[C:35]([CH3:42])([CH3:41])[C:36]([O:38][CH2:39][CH3:40])=[O:37]>>[CH3:41][C:35]([N:15]1[CH2:16][CH2:17][N:12]([CH2:11][C:10]2[N:2]([CH3:1])[C:3]3[C:8]([N:9]=2)=[C:7]([N:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[N:6]=[C:5]([N:24]2[C:28]4[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=4[N:26]=[C:25]2[CH3:33])[N:4]=3)[CH2:13][CH2:14]1)([CH3:42])[C:36]([O:38][CH2:39][CH3:40])=[O:37]Participants
3
Procedure
Following General Procedure C, 4-(9-methyl-2-(2-methyl-1H-benzo[d]imidazol-1-yl)-8-(piperazin-1-ylmethyl)-9H-purin-6-yl)morpholine was alkylated with ethyl 2-bromo-2-methyl-propionate to give 502. LCMS m/z: 281.7 (2M+H+)
Sources & evidence
- ORD record
- ord-c160037ba1bc4ec1aee389cc4b09140a
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08173650B2
Reaction notes
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