1-Bromopropane → HCID 58980991, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][N:12]1[C:20]([C:21]2[N:22]([CH3:26])[CH:23]=[CH:24][N:25]=2)=[C:19]2[C:14]([NH:15][C:16](=[O:29])[N:17]([CH3:28])[C:18]2=[O:27])=[N:13]1.Br[CH2:31][CH2:32][CH3:33].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][N:12]1[C:20]([C:21]2[N:22]([CH3:26])[CH:23]=[CH:24][N:25]=2)=[C:19]2[C:14]([N:15]([CH2:31][CH2:32][CH3:33])[C:16](=[O:29])[N:17]([CH3:28])[C:18]2=[O:27])=[N:13]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound was synthesized by the reaction of 2-[(5-chloro-1H-indol-3-yl)methyl]-5-methyl-3-(1-methyl-1H-imdazol-2-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione and 1-bromopropane using potassium carbonate as a base in DMF at 80° C. Mass: 452.08 (M+H).
Workup
- customat 80° C
Sources & evidence
- ORD record
- ord-accf7ce7362249b194c08da1248c6ae3
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285558B2
Reaction notes
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