Acetone → HCID 68984339, compound
Reaction equation
[CH2:1]([N:5]([CH:30]1[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1)[C:6]1[C:7]([O:28][CH3:29])=[N:8][N:9]2[C:13]([C:14]3[C:19]([O:20][CH3:21])=[CH:18][C:17]([CH2:22][O:23][CH2:24][CH3:25])=[CH:16][C:15]=3[O:26][CH3:27])=[CH:12][S:11][C:10]=12)[CH2:2][CH2:3][CH3:4].CC(C)=O.[BrH:40]>O>[BrH:40].[CH2:1]([N:5]([CH:30]1[CH2:31][CH2:32][O:33][CH2:34][CH2:35]1)[C:6]1[C:7]([O:28][CH3:29])=[N:8][N:9]2[C:13]([C:14]3[C:15]([O:26][CH3:27])=[CH:16][C:17]([CH2:22][O:23][CH2:24][CH3:25])=[CH:18][C:19]=3[O:20][CH3:21])=[CH:12][S:11][C:10]=12)[CH2:2][CH2:3][CH3:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To N-butyl-3-[4-(ethoxymethyl)-2,6-dimethoxyphenyl]-6-methoxy-N-(tetrahydro-2H-pyran-4-yl)pyrazolo[5,1-b][1,3]thiazole-7-amine (1.02 g) was added acetone (2 mL) warmed by hot water, then hydrobromic acid (8.84M, 240 μL) was added, and the mixture was stirred. The solvent in the mixture was partially removed by blowing nitrogen stream, and the mixture was further stirred.
Workup
- customThe solvent in the mixture was partially removed
Sources & evidence
- ORD record
- ord-4e48fd961bcc471880c0ab8bbf5ae968
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08431603B2
Reaction notes
Loading…