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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2190660생성일: 2026년 10월 26일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-{4-[5-(3-Iodo-4-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/2190660

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물N-(3-Iodo-4-methyl-phenyl)-6-piperazin-1-yl-nicotinamideHCID 59318071—
반응물HCID 178525731HCID 178525731—
용매DimethylformamideHCID 6228—
생성물4-{4-[5-(3-Iodo-4-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclohexanecarboxylic acidHCID 5931799312.4%

반응 단계

A mixture of N-(3-iodo-4-methyl-phenyl)-6-piperazin-1-yl-nicotinamide (60 mg, 0.14 mmol), trans-1,4-cyclohexane dicarboxylic acid (122 mg, 0.71 mmol) in DMF (10 mL) was treated with EDCI (130 mg, 0.71 mmol). After stirring overnight the reaction mixture was partitioned between EtOAc and water. The water layer was made basic to pH 13 with solid NaOH. The EtOAc layer was removed and then the water layer was acidified to pH 5 with aq conc. HCl and extracted again with EtOAc. The EtOAc layer obtained after the latter extraction was dried over Na2SO4, filtered and concentrated to the product (10 mg, Yield: 12%). HRMS m/z calcd for C25H29N4O4I [M+H]+: 577.1306. Found: 577.1306.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08324385B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-7c51d01c96c04fc09b91fada97e578aa
출처 메모uspto-grants-2012_12