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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2246835생성일: 2026년 10월 27일

Dimethyl Sulfoxide → 10-[(2'-Methoxy-1,1'-biphenyl-4-yl)carbonyl]-n-[(1-methyl-1h-pyrrol-2-yl)methyl]-10,11-dihydro-5h-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxamide

https://huagongshe.com/reaction/2246835

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물(1-methyl-1H-pyrrol-2-yl)methanamineHCID 2776207—
반응물2,2,2-trichloro-1-{10-[(2'-methoxy-1,1'-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanoneHCID 16038407—
용매AcetonitrileHCID 6342—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물10-[(2'-Methoxy-1,1'-biphenyl-4-yl)carbonyl]-n-[(1-methyl-1h-pyrrol-2-yl)methyl]-10,11-dihydro-5h-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxamideHCID 1199985340.3%

반응 조건

온도80 °C

반응 단계

To a suspension of 2,2,2-trichloro-1-{10-[(2′-methoxy-1,1′-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone of Example 1 (1.175 g, 2.17 mmole) in acetonitrile (15 mL) was added (1-methyl-1H-pyrrol-2-yl)methylamine (0.263 g, 2.38 mmole) followed by dimethylsulfoxide (0.710 g, 9.06 mmole) and triethylamine (0.400 g, 4 mmole). The mixture was heated under nitrogen at 80° C. for 4 hours. The solvent was removed in vacuo, and the residue was flash chromatographed on silica Merck-60 using a gradient of 0-25% of ethyl acetate in dichloromethane, to provide a yellow foam that yields a solid (0.464 g) upon treatment with ethyl acetate and hexane, mp 148-150° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07687623B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-8a4f9b1cfbc84c51972a44d3dc84ab72
출처 메모uspto-grants-2010_03