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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea | HCID 10839478 | — |
| 반응물 | Ethanol hydrochloride | HCID 21887872 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea hydrochloride | HCID 67640260 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05728829 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-55f511a55d61454a83be8c226edee531 |
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| 출처 메모 | uspto-grants-1998_03 |
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