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HRID 41316作成日:2026年10月23日

Water → 4-{[(3S)-3-methyl-4-(2-pyridinylcarbonyl)-1-piperazinyl]sulfonyl}benzonitrile

https://huagongshe.com/ja/reaction/41316

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Cyanobenzenesulfonyl chlorideHCID 39497—
反応物DiisopropylethylamineHCID 81531—
反応物(2S)-2-methyl-1-(2-pyridinylcarbonyl)piperazine dihydrochlorideHCID 67222743—
溶媒DichloromethaneHCID 6344—
生成物4-{[(3S)-3-methyl-4-(2-pyridinylcarbonyl)-1-piperazinyl]sulfonyl}benzonitrileHCID 4461196050.8%

反応手順

To a solution of (2S)-2-methyl-1-(2-pyridinylcarbonyl)piperazine dihydrochloride (Description 16) (71 mg, 0.255 mmol) in DCM (3 ml) was added DIPEA (0.183 ml, 1.046 mmol) at room temperature and to it was slowly added 4-cyanobenzenesulfonyl chloride (56.6 mg, 0.281 mmol) and the resultant mixture then stirred for 3 h. 5 ml of water and 5 ml of DCM were added and the organic layer separated with a phase separation cartridge and then evaporated under vacuum. The crude material (120 mg) was purified via Biotage (12M silica column) using a gradient [i-hex/EtOAc] ([90/10] to [40/60]). The desired fractions were then collected and concentrated to dryness giving the title compound (48 mg) as a white solid.

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-dc0910905023484a84df89cc4a67cb1f
出典メモuspto-grants-2013_09