반응식
[S:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([NH2:21])[C:13]=1[O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:8]([OH:10])=[O:9])(=[O:4])(=[O:3])[NH2:2].[CH2:22]([CH2:26][C:27](=O)[CH3:28])[C:23]([CH3:25])=O>C(O)(=O)C>[S:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([N:21]2[C:27]([CH3:28])=[CH:26][CH:22]=[C:23]2[CH3:25])[C:13]=1[O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:8]([OH:10])=[O:9])(=[O:3])(=[O:4])[NH2:2]참가 물질
실험 절차
A mixture of 3-sulphamoyl-4-phenoxy-5-aminobenzoic acid (1.54 g=5 mmols; P. W. Feit, J. Med. Chem. 14, 432 (1971)), acetonylacetone (0.57 g=5 mmols) and 10 ml of glacial acetic acid is refluxed under N2 for 30 minutes, the red reaction solution is evaporated in vacuo and freed from residues of glacial acetic acid and water by adding benzene and evaporating azeotropically, the residue is dissolved in acetone, the solution is boiled with silica gel and filtered through a fine filter and the solution is concentrated to 50 ml and, after adding 50 ml of ethyl acetate, freed from acetone residues in vacuo, whereupon crystallisation takes place. After the purification procedure has been repeated, beige-coloured crystals with a melting point of 283°-286° (decomposition) result.
후처리
- temperatureis refluxed under N2 for 30 minutes
- customthe red reaction solution is evaporated in vacuo
- additionby adding benzene
- customevaporating azeotropically
- dissolutionthe residue is dissolved in acetone
- filtrationfiltered through
- filtrationa fine filter
- concentrationthe solution is concentrated to 50 ml
- additionafter adding 50 ml of ethyl acetate
- customfreed from acetone residues in vacuo, whereupon crystallisation
- customAfter the purification procedure
- custombeige-coloured crystals with a melting point of 283°-286° (decomposition) result
출처 및 근거
- ORD 기록
- ord-b4dd32f738804d1ab26ad29360b531ae
- 출처 데이터셋
- uspto-grants-1979_11
- 특허 번호
- US04176190
연결된 노트
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