Reaction equation
[CH3:1][NH:2][CH2:3][CH2:4][CH3:5].[CH3:6][O:7][C:8](=[O:19])[C:9]1[CH:17]=[C:16]([Br:18])[CH:15]=[C:11]([C:12]([OH:14])=O)[CH:10]=1.BrC1C=C(C(O)=O)C=C(C=1)C(O)=O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[Cl-].[NH4+].Cl>ClCCl>[CH3:6][O:7][C:8](=[O:19])[C:9]1[CH:17]=[C:16]([Br:18])[CH:15]=[C:11]([C:12]([N:2]([CH3:1])[CH2:3][CH2:4][CH3:5])=[O:14])[CH:10]=1Participants
Reactant 7
Product 1
Reagents, catalysts & solvents 1
Procedure
Add N-methylpropylamine (5.14 g, 70.4 mmol) to a mixture of 5-bromo-isophthalic acid monomethyl ester and 5-bromo-isophthalic acid (18.2 g), 1-hydroxybenzotriazole (9.5 g, 70.4 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (13.5 g, 70.4 mmol) in dichloromethane (200 mL). Stir the solution for 2 h at room temperature. Add saturated aqueous ammonium chloride (100 mL) and acidify the mixture with 1 N HCl. Filter away the precipitate, extract the filtrate with dichloromethane, wash the organic extracts with 1 N HCl, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 30:70 ethyl acetate:hexanes) to give the title compound as an oil (10.1 g, 46%).
Workup
- filtrationFilter away the precipitate
- extractionextract the filtrate with dichloromethane
- washwash the organic extracts with 1 N HCl, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride
- dry with materialdry (magnesium sulfate)
- concentrationconcentrate
- custompurify
- wash(silica gel chromatography, eluting with 30:70 ethyl acetate:hexanes)
Sources & evidence
- ORD record
- ord-b625701daee9445d956f5ada3581bf28
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585885B2
Linked notes
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