돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55233생성일: 2026년 10월 23일

Triethylamine → alpha-[N-(Acetamido)amino]-N-[4-(5H-pyrrolo[2,1-c][1,4]-benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide

https://huagongshe.com/ko/reaction/55233

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
반응물Glycinamide hydrochlorideHCID 2723639—
반응물alpha-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4)benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamideHCID 21837022—
용매MethanolHCID 887—
생성물alpha-[N-(Acetamido)amino]-N-[4-(5H-pyrrolo[2,1-c][1,4]-benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamideHCID 2183713685.8%

반응 조건

온도75 °C

반응 단계

A mixture of 0.14 g of α-chloro-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide, 0.17 g of glycinamide HCl, 0.15 g of triethylamine, 3 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone and 1 ml of methyl alcohol is heated at 75° C. for 2 days. The methyl alcohol is evaporated and the residue diluted with water. The resulting suspension is filtered and the precipitate washed with water. The solid is dissolved in ethyl acetate and washed with saturated NaHCO3, brine and dried with Na2SO4. The mixture is filtered and the filtrate evaporated in vacuo to a residue which is stirred with ether-hexanes to give 0.13 g of tan solid. MS(CI): 494(M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624923
출처 데이터셋uspto-grants-1997_04
ORD IDord-0b412438340a48aabf5d6522e3202962
출처 메모uspto-grants-1997_04