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HRID 750956作成日:2026年10月26日

Water → 4-[4-(4-{2-[(e)-2-(-4-Trifluoromethanesulfinyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1-trityl-1h-[1,2,3]triazole

https://huagongshe.com/reaction/750956

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物4-{4-[1-(Triphenylmethyl)-1H-1,2,3-triazol-4-yl]butyl}phenolHCID 23614547—
反応物4-Chloromethyl-2-[2-(4-trifluoromethylsulfinyl-phenyl)-vinyl]-oxazoleHCID 69292389—
溶媒DimethylformamideHCID 6228—
生成物4-[4-(4-{2-[(e)-2-(-4-Trifluoromethanesulfinyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1-trityl-1h-[1,2,3]triazoleHCID 69291936—

反応手順

8.1 mg (0.20 mmol) 95% sodium hydride were given at 0° C. to a solution of 90 mg (0.20 mmol) 4-[4-(1-trityl-1H-[1,2,3]triazol-4-yl)-butyl]-phenol in 3.0 ml N,N-dimethylformamide and stirred for 15 min. 66 mg (0.20 mmol) 4-chloromethyl-2-[2-(4-trifluoromethanesulfinyl-phenyl)-vinyl]-oxazole were added and stirring continued at 25° C. for 2 h. The reaction mixture was poured into water and extracted with ethyl acetate. The organic phase was dried over sodium sulphate and the solvents distilled off in vacuo. Yield 146 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07405231B2
出典データセットuspto-grants-2008_07
ORD IDord-93c8c8de96684188bfa8bb4362c956cb
出典メモuspto-grants-2008_07