돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41316생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-Cyanobenzenesulfonyl chlorideHCID 39497—
반응물DiisopropylethylamineHCID 81531—
반응물(2S)-2-methyl-1-(2-pyridinylcarbonyl)piperazine dihydrochlorideHCID 67222743—
용매DichloromethaneHCID 6344—
생성물4-{[(3S)-3-methyl-4-(2-pyridinylcarbonyl)-1-piperazinyl]sulfonyl}benzonitrileHCID 4461196050.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530478B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-dc0910905023484a84df89cc4a67cb1f
출처 메모uspto-grants-2013_09