Diisopropylethylamine → Acetic acid 4-[(5-isopropyl-[1,3,4]thiadiazol-2-yl)-(2-trimethylsilanyl-ethoxymethyl)-sulfamoyl]-phenyl ester
반응식
[CH:1]([C:4]1[S:8][C:7]([NH:9][S:10]([C:13]2[CH:18]=[CH:17][C:16]([O:19][C:20](=[O:22])[CH3:21])=[CH:15][CH:14]=2)(=[O:12])=[O:11])=[N:6][N:5]=1)([CH3:3])[CH3:2].C(N(CC)C(C)C)(C)C.[CH3:32][Si:33]([CH3:40])([CH3:39])[CH2:34][CH2:35][O:36][CH2:37]Cl>ClCCl.CN(C)C1C=CN=CC=1>[CH:1]([C:4]1[S:8][C:7]([N:9]([CH2:37][O:36][CH2:35][CH2:34][Si:33]([CH3:40])([CH3:39])[CH3:32])[S:10]([C:13]2[CH:18]=[CH:17][C:16]([O:19][C:20](=[O:22])[CH3:21])=[CH:15][CH:14]=2)(=[O:11])=[O:12])=[N:6][N:5]=1)([CH3:3])[CH3:2]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
3.3 g Acetic acid 4-(5-isopropyl-[1,3,4]thiadiazol-2-ylsulfamoyl)-phenyl ester were dissolved in 12 ml dichloromethane. 2.69 ml N,N-diisopropylethylamine, 78 mg 4-dimethylaminopyridine and 2.1 g 2-(trimethylsilyl)ethoxymethyl chloride were added. The reaction mixture was stirred at room temperature for one hour. The solvent was removed in vacuo and the residue purified by flash chromatography on silica gel with the eluents n-heptane:ethyl acetate=1:1=>1:3 to obtain 2.7 g acetic acid 4-[(5-isopropyl-[1,3,4]thiadiazol-2-yl)-(2-trimethylsilanyl-ethoxymethyl)-sulfamoyl]-phenyl ester.
후처리
- customThe solvent was removed in vacuo
- customthe residue purified by flash chromatography on silica gel with the eluents n-heptane
출처 및 근거
- ORD 기록
- ord-89c77b4874e346909e63c8197d0f79e7
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07910612B2
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