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HRID 43404作成日:2026年10月23日

Water → HCID 59161341、化合物

https://huagongshe.com/ja/reaction/43404

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4-Methylnicotinic acidHCID 229163—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物(S)-3-Methyl-1-((4-(trifluoromethyl)phenyl)sulfonyl)piperazineHCID 59152086—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物HCID 59161341HCID 5916134148.4%

反応手順

To a solution of (3S)-3-methyl-1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (Description 2) (100 mg, 0.324 mmol) in DMF (5 ml) was added HOBT.H2O (49.7 mg, 0.324 mmol), HBTU (123 mg, 0.324 mmol), 4-methyl-3-pyridinecarboxylic acid (44.5 mg, 0.324 mmol) and DIPEA (0.170 ml, 0.973 mmol) and the reaction mixture was stirred for 1 h at room temperature. The reaction mixture was reduced in vacuo. The residue was dissolved in DCM (50 ml), transferred to a separating funnel and the solution was washed with aqueous NaHCO3 (5 ml), twice. The organic layer was dried with dried magnesium sulphate which was removed by filtration and the filtrate evaporated to dryness in vacuo. The residual oil was dissolved in 1:1 MeCN/DMSO (1.8 ml) and purified by MDAP in two batches. The fractions containing the desired product were combined and evaporated to dryness in vacuo. The residue was then dissolved in diethyl ether (50 ml) and transferred to a 100 ml round bottom flask and reduced to dryness in vacuo to yield the title compound (67 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536183B2
出典データセットuspto-grants-2013_09
ORD IDord-96a0a363d25c44d89643925c156f5a7e
出典メモuspto-grants-2013_09