Carbon Dioxide → HCID 22477614, compound
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:16][C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[C:9]=2[CH3:17])=[CH:4][CH:3]=1.C([Li])CCC.[C:23](=[O:25])=[O:24]>C1COCC1>[C:23]([C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:16][C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[C:9]=2[CH3:17])=[CH:4][CH:3]=1)([OH:25])=[O:24]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(p-Bromophenyl)-3-methyl-pyrrolo-[2,3 -b]pyridine (1 g, 3.5 mmol) was dissolved in 200 ml dry THF, deaerated and cooled to -78° C. n-Butyllithium (5.19 ml, 8.4 mmol) was added dropwise and the mixture was allowed to reach room temperature CO2 (g) was bubbled through the solution for 10 min.
Workup
- additionwas added dropwise
- customto reach room temperature
- customwas bubbled through the solution for 10 min.
Sources & evidence
- ORD record
- ord-9ec4d62124464b65926d6843428abd6c
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05439917
Reaction notes
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