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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77779생성일: 2026년 10월 24일

N-methyl-2-pyrrolidone → 4'-Methyl-5-(5-methyl-tetrazol-1-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide

https://huagongshe.com/ko/reaction/77779

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물MethoxyisopropylamineHCID 123458—
반응물4'-Methyl-5-(5-methyl-tetrazol-1-yl)-biphenyl-3-carboxylic acidHCID 57850935—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4'-Methyl-5-(5-methyl-tetrazol-1-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 5785125590%

반응 단계

To a stirred solution of 4′-methyl-5-(5-methyl-tetrazol-1-yl)-biphenyl-3-carboxylic acid (0.3402 mmol, 100 mg), HOBt (0.6804 mmol, 91.9 mg), 2-methoxy-1-methyl-ethylamine (0.4083 mmol, 43 μL) and NMP (1.0206 mmol, 112 μL) in CH2Cl2 (1 mL) and DMF (0.5 mL) was added EDCI (0.6804 mmol, 130.4 mg) at room temperature, and the mixture was stirred at room temperature for 18 hours. The mixture was extracted with ethyl acetate and the organic layer was washed with 2N aqueous NaOH, 1 N aqueous HCl, brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by Flash column chromatography, eluting with n-hexane:ethyl acetate (4:1) to give 4′-methyl-5-(5-methyl-tetrazol-1-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (white powder, 90% yield). MS (M+H)=366.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841336B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-33b87137c5644306b8efb80d7344d64c
출처 메모uspto-grants-2014_09