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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263217생성일: 2026년 10월 26일

(1-Isopropylpiperidin-4-yl)methanamine → 2-Chloropropane

https://huagongshe.com/reaction/263217

반응식

참여 물질

역할이름HCID투입량
반응물(1-Isopropylpiperidin-4-yl)methanamineHCID 7258859—
반응물3-Chloro-6-chlorocarbonylphenylsulfenyl chlorideHCID 10728826—
생성물2-ChloropropaneHCID 6361—
생성물N-(piperidin-4-ylmethyl)acetamideHCID 4341747—

반응 단계

2-(1-sopropylpiperid-4-ylmethyl)-6-chloro-1,2-benzisothiazolin-3-one is obtained analogously to Example 33 by reacting 3-chloro-6-chlorocarbonylphenylsulfenyl chloride and 1-isopropyl-4-aminomethylpiperidine [boiling point 15 :95°-97° C.; obtained from 4-acetylaminomethylpiperidine and isopropyl chloride analogously to Singh et al., J. Med. Chem. 12, 949 (1969) and Werbel et al., supra]. After recrystallization in acetone, yellow crystals of melting point 134°-135° C. are obtained; yield: 37% of theory.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04156729
출처 데이터셋uspto-grants-1979_05
ORD IDord-96feb2b4c82e4f69ac86803b109e0cef
출처 메모uspto-grants-1979_05