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HRID 41313作成日:2026年10月24日

Water → 1-[(2-Methyl-4-pyridinyl)carbonyl]-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine

https://huagongshe.com/ja/reaction/41313

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物1-[4-(Trifluoromethyl)benzenesulfonyl]piperazineHCID 2554578—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物2-Methylpyridine-4-carboxylic acidHCID 2762821—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1-[(2-Methyl-4-pyridinyl)carbonyl]-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazineHCID 4461208057.6%

反応手順

To a solution of 1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (Description 1) (100 mg, 0.340 mmol) in DMF (5 ml) was added HOBT.H2O (52.0 mg, 0.340 mmol), HBTU (129 mg, 0.340 mmol), 2-methyl-4-pyridinecarboxylic acid (46.6 mg, 0.340 mmol) and DIPEA (0.178 ml, 1.02 mmol). The reaction mixture was stirred for 2 hours at room temperature. Reaction mixture was transferred to a 100 ml round bottom flask and was reduced to dryness in vacuo. The residue was dissolved in DCM (50 ml) and was transferred to a separating funnel then washed with saturated NaHCO3 solution (5 ml), twice. The organic layer was collected and dried with magnesium sulphate. The solid was removed by filtration and the filtrate collected in a 250 ml round bottom flask and reduced to dryness in vacuo. The residue was then dissolved in 1.8 ml 1:1 MeCN/DMSO and purified by MDAP in 2 batches. The fractions containing desired product were combined in a 250 ml round bottom flask and reduced in vacuo to yield the title compound (81 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530478B2
出典データセットuspto-grants-2013_09
ORD IDord-8dc7e5fd601245d8a35ff0dac3ebe8f0
出典メモuspto-grants-2013_09