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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77754생성일: 2026년 10월 24일

N-methyl-2-pyrrolidone → 3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide

https://huagongshe.com/ko/reaction/77754

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Iodo-5-nitrobenzoic acidHCID 80580—
반응물MethoxyisopropylamineHCID 123458—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamideHCID 5785131927.9%

반응 단계

EDCI (7.07 g, 36.9 mmol) was added in one portion to a stirred solution of 3-Iodo-5-nitro-benzoic acid (2.31 g, 24.6 mmol), HOBt (4.985 g, 36.9 mmol), 2-Amino-1-methoxypropane (2.73 ml, 24.6 mmol) and NMP (4.06 ml 36.9 mmol) in CH2Cl2 (120 ml) and DMF (10 ml) at 0° C. The reaction was allowed to warm to room temperature and was stirred over night. The reaction mixture was then washed with 2N NaOH, water, brine, and dried over Na2SO4. Solvent was removed in vacuo to give 2.50 g of 3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide as a yellow solid, MS (M+H)=365. This material was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841336B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6fb4a07699894e098ba180e9330902a7
출처 메모uspto-grants-2014_09