돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53242생성일: 2026년 10월 25일

Diisopropylethylamine → N-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)methanesulfonamide

https://huagongshe.com/reaction/53242

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N-(2-bromoethyl)methanesulfonamideHCID 285330—
반응물4-PiperidinemethanolHCID 420771—
용매AcetonitrileHCID 6342—
생성물N-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)methanesulfonamideHCID 1996211454.8%

반응 단계

4-Piperidine methanol (1.60 g) was dissolved in dry acetonitrile (40 ml), N,N-diisopropylethylamine (5 ml) was added, followed by N-(2-bromoethyl)methanesulphonamide (2.95 g) in acetonitrile (10 ml), and the resulting mixture heated at reflux for 2 h. The solvent was removed in vacuo to leave a gum. This was purified by FCC eluting with System A (75:8:1) to give the title compound (1.80 g) as a solid, m.p. 81°-82°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618827
출처 데이터셋uspto-grants-1997_04
ORD IDord-b799967ecb2b40aeb1be5ec9736eebe1
출처 메모uspto-grants-1997_04