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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2077516생성일: 2026년 10월 23일

Sodium Carbonate Monohydrate → N-(7-(3-Fluoro-4-methoxyphenyl)benzo[d]thiazol-2-yl)acetamide

https://huagongshe.com/ko/reaction/2077516

반응식

참여 물질

역할이름HCID투입량
반응물Sodium Carbonate MonohydrateHCID 2735133—
반응물3-Fluoro-4-methoxyphenylboronic acidHCID 2782194—
반응물N-(6-bromo-1,3-benzothiazol-2-yl)acetamideHCID 3240669—
반응물N-(7-bromobenzo[d]thiazol-2-yl)acetamideHCID 57584914—
촉매HCID 178418476HCID 178418476—
용매EthanolHCID 702—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-(7-(3-Fluoro-4-methoxyphenyl)benzo[d]thiazol-2-yl)acetamideHCID 57584946—
생성물N-(6-(3-Fluoro-4-methoxyphenyl)benzo[d]thiazol-2-yl)acetamideHCID 86627994—

반응 조건

온도85 °C

반응 단계

The mixture (302.6 mg, 1.116 mmol) of N-(7-bromobenzo[d]thiazol-2-yl)acetamide and N-(6-bromobenzo[d]thiazol-2-yl)acetamide, 3-fluoro-4-methoxyphenylboronic acid (298 mg, 1.75 mmol), sodium carbonate monohydrate (0.247 mL, 4.48 mmol), and dichlorobis(triphenylphosphine)palladium (II) (168 mg, 0.239 mmol) were suspended in 1,2-dimethoxyethane (3.5 mL), water (1.5 mL) and EtOH (1.0 mL). The reaction flask was fit with a reflux condensor and placed in a preheated oil bath (85° C.) and stirred under argon for 1 hour. The reaction was cooled to room temperature and allowed to stand overnight. It was then filtered through a Celite® (diatomaceous earth) pad, and the solid was washed with MeOH, DCM, and DME. The filtrate was concentrated and treated with DCM. The resulting precipitate was collected by filtration and the crude was further purified by HPLC to provide N-(7-(3-Fluoro-4-methoxyphenyl)benzo[d]thiazol-2-yl)acetamide and N-(6-(3-Fluoro-4-methoxyphenyl)benzo[d]thiazol-2-yl)acetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07928140B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-79222293d2ca422582a2e4ede6183025
출처 메모uspto-grants-2011_04