돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238621생성일: 2026년 10월 24일

2-Bromo-5-(ethylsulfonyl)pyridine → [4-(5-Ethanesulfonyl-pyridin-2-yloxy)-3,6-difluoro-naphthalen-2-yl]-acetic acid methyl ester

https://huagongshe.com/ko/reaction/238621

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-5-(ethylsulfonyl)pyridineHCID 53393184—
반응물(3,6-Difluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl esterHCID 59326617—
반응물2-(4-Fluoro-benzylidene)-succinic acid 1-methyl esterHCID 67303799—
생성물[4-(5-Ethanesulfonyl-pyridin-2-yloxy)-3,6-difluoro-naphthalen-2-yl]-acetic acid methyl esterHCID 5932647748%

반응 단계

Starting with (3,6-difluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl ester (25 mg, 0.099 mmol) and 2-bromo-5-ethanesulfonyl-pyridine (28 mg, 0.112 mmol), using a method analogous to the one described for the methyl ester of example 1-1, [4-(5-ethanesulfonyl-pyridin-2-yloxy)-3,6-difluoro-naphthalen-2-yl]-acetic acid methyl ester (20 mg, 48%) was obtained as a white solid, which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642629B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-1ba199307a4f4c2e99abaff2eacf5524
출처 메모uspto-grants-2014_02