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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 424881생성일: 2026년 10월 26일

1-Methylimidazole → (S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide

https://huagongshe.com/reaction/424881

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물3-Benzoylpropionic acidHCID 72871—
반응물(S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamineHCID 57943187—
용매DichloromethaneHCID 6344—
생성물(S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamideHCID 59464671—

반응 단계

3-Benzoylpropionic acid (0.250 g) is dissolved in CH2Cl2 (5 mL), N-methyl imidazole (0.333 mL) is added and the resulting solution is cooled to 0° C. after which a solution of p-toluenesulfonyl chloride (0.320 g) in CH2Cl2 (2 mL) is added dropwise. After 0.5 hours (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine, 3, (0.388 g) is added. The reaction is stirred for 18 hours at room temperature and then concentrated in vacuo. The resulting residue is dissolved in EtOAc and washed with 1N HCl and brine. The solution is dried over Na2SO4, filtered, and concentrated and the crude material purified over silica to afford 0.415 g of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08106078B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-6b0e7d0dd83147b2a4c466ddbd9eada2
출처 메모uspto-grants-2012_01