Reaction equation
[CH3:1][O:2][C:3](=[O:24])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([NH2:16])=[C:12]([NH:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:11]=1.[CH3:25][O:26][C:27](OC)(OC)OC.[OH-].[Na+]>C(O)(=O)C>[CH3:1][O:2][C:3](=[O:24])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]2[N:16]=[C:25]([O:26][CH3:27])[N:17]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:12]=2[CH:11]=1Participants
5
Procedure
200 mg of 6-(3-phenylamino-4-aminophenyl)oxyhexanoic acid methyl ester was mixed with 0.12 ml of tetramethylorthocarbonate and 40 μl of acetic acid, and the mixture was heated for 4 hours to 80° C. After cooling, it was mixed with 1N sodium hydroxide solution, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 104 mg was obtained.
Workup
- temperaturethe mixture was heated for 4 hours to 80° C
- temperatureAfter cooling
- extractionextracted three times with ethyl acetate
- washthe combined organic phases were washed with saturated sodium chloride solution
- customdried on sodium sulfate
- concentrationconcentrated by evaporation in a vacuum
- customThe residue was purified by column chromatography on silica gel
- custom104 mg was obtained
Sources & evidence
- ORD record
- ord-cc4cad887e00467faafc24f3bc557a5f
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196202B2
Linked notes
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