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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1055329생성일: 2026년 10월 25일

Dimethyl Sulfoxide → Biphenyl-2-ylcarbamic Acid 1-(2-{[4-(4-Formyl-2,5-dimethylphenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl Ester

https://huagongshe.com/reaction/1055329

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참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물Biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-hydroxymethyl-2,5-dimethylphenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl esterHCID 66770430—
용매DichloromethaneHCID 6344—
생성물Biphenyl-2-ylcarbamic Acid 1-(2-{[4-(4-Formyl-2,5-dimethylphenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl EsterHCID 86646967—

반응 조건

온도0 °C

반응 단계

To a stirred solution of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-hydroxymethyl-2,5-dimethylphenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl ester (0.460 g, 0.748 mmol) and dimethyl sulfoxide (0.531 mL, 7.48 mmol) in DCM (2.58 mL) at 0° C. was added N,N-diisopropylethylamine (0.65 mL, 3.7 mmol). Sulfur trioxide —pyridine complex (0.357 g, 2.24 mmol) was added and the resulting mixture was stirred at 0° C. for 1 h. Water (3 mL) was added and the layers were separated. The organic layer was dried over sodium sulfate and filtered to give the title compound in a DCM solution, which was used immediately in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394275B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-64d13b445b6242f4aeedf760a8c46578
출처 메모uspto-grants-2016_07