돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323169생성일: 2026년 10월 23일

Diethyl Ether → 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[3-(4-methylpiperazin-1-ylcarbonyl)aminoprop-1-yl]phenyl]benzamide

https://huagongshe.com/ko/reaction/323169

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Sodium borohydrideHCID 4311764—
반응물4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[3-(4-methylpiperazin-1-yl)carbonylamino-(1-propyn-1-yl)]phenyl]benzamideHCID 70070182—
촉매Dichloronickel;hexahydrateHCID 11791229—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[3-(4-methylpiperazin-1-ylcarbonyl)aminoprop-1-yl]phenyl]benzamideHCID 2201056229.8%

반응 단계

To an ice cooled mixture of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[3-(4-methylpiperazin-1-yl)carbonylamino-(1-propyn-1-yl)]phenyl]benzamide (250 mg) and nickel chloride hexahydrate (297 mg) in a mixture of tetrahydrofuran (5 ml) and methanol (5 ml) was added sodium borohydride in small portions and the mixture was stirred at the same temperature for 1 hour. The mixture was filtered through bed of Celite and the filtrate was evaporated in vacuo. The residue was dissolved in chloroform (20 ml) and washed with water and brine. The organic solution was dried over magnesium sulfate and the solvent was evaporated in vacuo to give a syrup. The residue was solidified with diethyl ether to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[3-(4-methylpiperazin-1-ylcarbonyl)aminoprop-1-yl]phenyl]benzamide (75.0 mg) as a powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211242B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-e9f4748e503148fcb5e4ea2d6bc5ad00
출처 메모uspto-grants-2001_04