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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1585697생성일: 2026년 10월 25일

4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidine → N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide

https://huagongshe.com/reaction/1585697

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidineHCID 19353553—
반응물N-(4-sulfamoyl-phenyl)-acetamide potassium saltHCID 70262342—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 1064441466%

반응 단계

0.58 g (0.00266 mol) of 4,6-dichloro-2-pyrrolidin-1-yl-pyrimidine and 1.36 g (0.00539 mol) of N-(4-sulfamoyl-phenyl)-acetamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone at 140° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water and extracted. The aqueous phase was made acid with 4N HCl and extracted with ethyl acetate. Both organic phases were combined and concentrated. The residue was recrystallized from a small amount of ethanol and the mother liquor was chromatographed over silica gel with cyclohexane/ ethyl acetate 2:1 as the eluent. There was obtained a total of 0.62 g (66%) of N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide as whitish crystals; m.p. 229-233° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05939451
출처 데이터셋uspto-grants-1999_08
ORD IDord-a64a02ecd5154747ba15c3d5b604bcaf
출처 메모uspto-grants-1999_08