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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2340생성일: 2026년 10월 23일

N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea → N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea hydrochloride

https://huagongshe.com/ko/reaction/2340

반응식

참여 물질

역할이름HCID투입량
반응물N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)ureaHCID 10839478—
반응물Ethanol hydrochlorideHCID 21887872—
용매EthanolHCID 702—
생성물N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea hydrochlorideHCID 67640260—

반응 조건

온도50 °C

반응 단계

N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea (70 g, 136.6 mmol) was taken up in ethanol (1 l) and 2.26M HCl ethanol (63.5 ml, 143.4 mmol) was added dropwise. The mixture was warmed up to 50° C. to afford a clear solution, which was seeded, cooled to 0° C. and stirred at the same temperature overnight. The resultant precipitate was collected by flirtation to provide the title compound as a white crystalline (62.4 g, 82%): top. 181°-184° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728829
출처 데이터셋uspto-grants-1998_03
ORD IDord-55f511a55d61454a83be8c226edee531
출처 메모uspto-grants-1998_03