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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8602생성일: 2026년 10월 25일

4,6-Dichloro-5-(2-methoxyphenoxy)-2-(pyridin-4-YL)pyrimidine → 2-Phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/8602

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-5-(2-methoxyphenoxy)-2-(pyridin-4-YL)pyrimidineHCID 11175458—
반응물2-Phenyl-ethanesulfonic acid amide potassium saltHCID 68898150—
용매DimethylformamideHCID 6228—
생성물2-Phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amideHCID 8659247178.1%

반응 단계

A solution of 4,6-dichloro-5-(2-methoxyphenoxy)-2-(4-pyridyl)-pyrimidine (2 g) and 2-phenyl-ethanesulfonic acid amide potassium salt (2.82 g, Referential Example 1e) in DMF (50 ml) was stirred at rt for 16 h. Bulk of the solvent was evaporated before it was diluted with diethyl ether (50 ml). The mixture was acidified with 10% aq. citric acid. The precipitate that formed was collected, washed with diethyl ether (100 ml) and dried to give 2-phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide (2.23 g) as a beige powder. LC-MS: tR=4.93 min, [M+1]+=497.22, [M−1]−=494.96.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091201B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-50ab374672784712afdda58eb7ef9ef4
출처 메모uspto-grants-2006_08