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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 575269생성일: 2026년 10월 26일

10-bromo-3((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide → (R)-10-((3-hydroxy-1-methyl-2-oxopyrrolidin-3-yl)ethynyl)-3-((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide

https://huagongshe.com/reaction/575269

반응식

참여 물질

역할이름HCID투입량
반응물10-bromo-3((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamideHCID 86693288—
반응물(R)-3-ethynyl-3-hydroxy-1-methylpyrrolidin-2-oneHCID 86693296—
촉매HCID 178418397HCID 178418397—
용매Dimethyl SulfoxideHCID 679—
생성물(R)-10-((3-hydroxy-1-methyl-2-oxopyrrolidin-3-yl)ethynyl)-3-((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamideHCID 8669329519%

반응 단계

Similar to as described in General Procedure E with the exceptions of using Pd(PPh3)4 in DMSO, 10-bromo-3-((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide was reacted with (R)-3-ethynyl-3-hydroxy-1-methylpyrrolidin-2-one to yield the titled compound as a yellow solid (21 mg, 19%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034866B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-5196f80411df498c84b7d4b2984b16a9
출처 메모uspto-grants-2015_05