HCID 67086685, compound → HCID 67286401, compound
Reaction equation
C[O:2][C:3](=[O:23])[C:4]1[CH:9]=[C:8]([O:10][CH3:11])[C:7]([O:12][CH2:13][CH2:14][N:15]2[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]2)=[C:6]([Cl:22])[CH:5]=1>[OH-].[Na+].C1COCC1>[Cl:22][C:6]1[CH:5]=[C:4]([CH:9]=[C:8]([O:10][CH3:11])[C:7]=1[O:12][CH2:13][CH2:14][N:15]1[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]1)[C:3]([OH:23])=[O:2]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 3-Chloro-5-methoxy-4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzoic acid methyl ester (3.7 g, 10.7 mmol) in 2 N NaOH (20 ml) and THF (40 ml) is heated at reflux for 1 hour. The reaction mixture is washed with Et2O. The aqueous phase is concentrated in vacuo, and water (50 ml) is added. The pH is adjusted to 3-4 using 2 N HCl. To this solution is added DOWEX 50WX4 (previously washed with MeOH, 2 N HCl and water), and the resulting mixture is stirred at room temperature for 1 hour. The resin is filtered, washed with water, and the product is released from the resin by washing with MeOH/NH4OH. The solution is concentrated in vacuo, diluted with DCM and MeOH, dried (Na2SO4) and the solvent removed in vacuo to yield the title compound as a light cream solid.
Workup
- temperatureat reflux for 1 hour
- washThe reaction mixture is washed with Et2O
- concentrationThe aqueous phase is concentrated in vacuo, and water (50 ml)
- additionis added
- additionTo this solution is added DOWEX 50WX4 (
- washpreviously washed with MeOH, 2 N HCl and water), and the resulting mixture
- filtrationThe resin is filtered
- washwashed with water
- washby washing with MeOH/NH4OH
- concentrationThe solution is concentrated in vacuo
- additiondiluted with DCM and MeOH
- dry with materialdried (Na2SO4)
- customthe solvent removed in vacuo
Sources & evidence
- ORD record
- ord-262f9525bbcb45c78feebf3e33aae61e
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08697687B2
Reaction notes
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