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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2252727생성일: 2026년 10월 27일

Hydrochloric Acid → Ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amide

https://huagongshe.com/reaction/2252727

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4,6-Dichloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidineHCID 10545706—
반응물Ethanesulfonamide potassium saltHCID 59645266—
용매Dimethyl SulfoxideHCID 679—
생성물Ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 5964527183.2%

반응 단계

To a solution of 4,6-dichloro-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl (prepared as described in [6] and [11]) (1.74 g) in DMSO (5 ml) was added ethanesulfonamide potassium salt (1.62 g). Stirring was continued for 10 days at rt. The reaction mixture was poured onto ice/water and acidified by 2N HCl. The precipitate was filtered off, washed with water and dried at HV to give ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (1.75 g) as a white powder. LC-MS: tR: 3.77, [M+H]+: 422.15.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07323465B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-1833bfeb75884697a5a22960994186ed
출처 메모uspto-grants-2008_01