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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879351생성일: 2026년 10월 26일

N-Propyl-Methyl Piperidinium Bis(trifluoroMethylsulfonyl)Imide → (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(1-(trifluoromethyl)-1H-indazol-5-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetate

https://huagongshe.com/reaction/879351

반응식

참여 물질

역할이름HCID투입량
반응물N-Propyl-Methyl Piperidinium Bis(trifluoroMethylsulfonyl)ImideHCID 4176748—
반응물3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxoleHCID 16043572—
반응물(S)-ethyl 2-(2-(2-(1H-indazol-5-yl)pyridin-4-yl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetateHCID 86700148—
용매Carbon DisulfideHCID 6348—
생성물(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(1-(trifluoromethyl)-1H-indazol-5-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetateHCID 86700151—

반응 단계

To a solution of (S)-ethyl 2-(2-(2-(1H-indazol-5-yl)pyridin-4-yl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate (40 mg, 0.065 mmol) in CS2 (1.5 mL), was added 1-Trifluoromethyl-3,3-dimethyl-1,2-benziodoxole (64 mg, 0.195 mmol), bis(trifluoromethane)sulfonimide (27 mg, 0.0975 mmol). The reaction mixture was heated at 60° C. in sealed microwave vial for 1d. The reaction mixture was washed by saturated NaHCO3, extracted by EtOAc, the organic phase was dried over MgSO4, filtered, concentrated down, purified by silica gel column, eluting by 0-50% EtOAc in hexanes to give the product. LCMS-ESI+: calc'd for C35H30ClF3N4O3S: 679.2 (M+H+); found: 679.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987250B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-290f9bc16bda4745ad44641c63c11cbe
출처 메모uspto-grants-2015_03