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HRID 5787생성일: 2026년 10월 23일

Thiophosgene → 2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole

https://huagongshe.com/ko/reaction/5787

반응식

참여 물질

역할이름HCID투입량
반응물ThiophosgeneHCID 10040—
반응물Potassium BicarbonateHCID 516893—
반응물6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 19794186—
용매ChloroformHCID 6212—
생성물2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 15610362—

반응 단계

To a cooled mixture of 2.1 g of 6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole and 2.8 g of potassium bicarbonate in 20 ml of chloroform is added dropwise 1.6 g of thiophosgene in 5 ml of chloroform under stirring. The stirring is continued for 2 hours maintaining the temperature at 0°-2° . The solid is filtered and the filtrate is evaporated. The solid thus obtained is dissolved in chloroform and filtered through a silica gel column. The filtrate is evaporated to give 2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole, melting at 54°-58°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246927
출처 데이터셋uspto-grants-1993_09
ORD IDord-6cc07c4d63d84829877b5eb5f5957d9d
출처 메모uspto-grants-1993_09