돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5786생성일: 2026년 10월 25일

2-Tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazole → 6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole

https://huagongshe.com/reaction/5786

반응식

참여 물질

역할이름HCID투입량
반응물2-Tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazoleHCID 19794189—
촉매NickelHCID 935—
용매MethanolHCID 887—
생성물6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 19794186—

반응 단계

A solution of 15.2 g of 2-tert-butyl-5-(4-methyl-piperidin-1-yl)-6-nitrobenzothiazole in 600 ml of methanol is hydrogenated in presence of 6.5 g of Raney Nickel at room temperature. After removing the catalyst the solution is concentrated and the solid filtered to give 6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole melting at 146°-148°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246927
출처 데이터셋uspto-grants-1993_09
ORD IDord-d2d2589cd1d140879dce79874d0e6100
출처 메모uspto-grants-1993_09