돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854390생성일: 2026년 10월 27일

((Chloromethyl)sulphonyl)benzene → 1-Methyl-4-{5-nitro-6-[(phenylsulfonyl)methyl]pyridin-2-yl}piperazine

https://huagongshe.com/reaction/854390

반응식

참여 물질

역할이름HCID투입량
반응물((Chloromethyl)sulphonyl)benzeneHCID 81625—
반응물1-Methyl-4-(5-nitropyridin-2-yl)piperazineHCID 2764066—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물1-Methyl-4-{5-nitro-6-[(phenylsulfonyl)methyl]pyridin-2-yl}piperazineHCID 5893406985%

반응 조건

온도-10 °C

반응 단계

A stirred solution of 1-methyl-4-(5-nitropyridin-2-yl)piperazine (1.10 g, 5.00 mmol) and chloromethylphenylsulfone (0.950 g, 5.00 mmol) in dry THF, under nitrogen, is cooled to −60° C., treated with 1.0 M KOtBu in THF (10.0 mL, 10.0 mmol), allowed to warm to −10° C. over a 1 h period, quenched with acetic acid, treated sequentially with water and saturated aqueous NaHCO3 and extracted with CH2Cl2. The combined extracts are washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is crystallized from EtOAc to give the title compound as a yellow solid, 1.60 g (85% yield), mp: 170°-172° C., identified by mass spectral and NMR analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259165B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-b2b1b7e7168c4801a901b747bde79773
출처 메모uspto-grants-2007_08