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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338521생성일: 2026년 10월 25일

Methanesulfonamide → 6-chloro-5-[4-(1-hydroxycyclobutyl)phenyl]-N-(methylsulfonyl)-1H-indole-3-carboxamide

https://huagongshe.com/reaction/338521

반응식

참여 물질

역할이름HCID투입량
반응물MethanesulfonamideHCID 72879—
반응물3-Iodo-1,2-phenylene bis(2,2-dimethylpropanoate)HCID 53431101—
반응물6-Chloro-5-(4-(1-hydroxycyclobutyl)phenyl)-1H-indole-3-carbaldehydeHCID 86698568—
용매Isopropyl AcetateHCID 7915—
생성물6-chloro-5-[4-(1-hydroxycyclobutyl)phenyl]-N-(methylsulfonyl)-1H-indole-3-carboxamideHCID 7176798613%

반응 조건

온도80 °C

반응 단계

To a mixture of 6-chloro-5-[4-(1-hydroxycyclobutyl)phenyl]-1H-indole-3-carbaldehyde (40 mg, 0.123 mmol), Bis(tert-butylcarbonyloxy)iodobenzene (104 mg, 0.256 mmol) in isopropyl acetate (2 mL) was added methanesulfonamide (12 mg, 0.126 mmol). After stirring 5 minutes, Bis[rhodium(α,α,α′,α′-tetramethyl-1,3-benzenedipropionic acid)] (5 mg, 0.007 mmol) was added and heated to 80° C. overnight. The mixture was concentrated to give a crude residue, which was purified by preparative HPLC to afford the title compound (6.6 mg, 13%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889730B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-fd553db09de74a4e80ee05974710c584
출처 메모uspto-grants-2014_11