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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29509생성일: 2026년 10월 24일

1-Methylimidazole → (2-amino-5-chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanone

https://huagongshe.com/ko/reaction/29509

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물2-Amino-5-chlorobenzoic acidHCID 12476—
반응물Ammonium ChlorideHCID 25517—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물(2-amino-5-chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanoneHCID 1099897713.7%

반응 단계

To a solution of nBuLi (0.0730 mol) in hexane was added N-methyl imidazole (0.0608 mol) drop wise at -40° C. over 30 min under a nitrogen atmosphere. The resulting yellow solution was stirred for a further 3 hr at rt, and then refluxed for 1 h. 2-amino-5-chlorobenzoic acid (1.74 g, 0.01014 mole) in dry ether (60 ml) was then added to the reaction mixture. The reaction mixture was stirred overnight at rt. To the reaction mixture was added saturated NH4Cl solution and the resulting mixture extracted with ethyl acetate (2×150 ml). The combined organic layers were dried over Na2SO4. After removal of solvent, the residue was purified by the flash chromatography using ethyl acetate/hexane (1:4) as eluent. Crystallization of the product from Et2O/hexane mixture gave 300 mg (13.7%) of product as yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-435f973cdb9d4431b3d43eeefb9a3641
출처 메모uspto-grants-2008_09