홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Bromine → 3,7-dibromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

HRID 17854
노트
인쇄 미리보기

반응식

HRID 17854 반응식
N1C2C=CC=CC=2CCCC1.[Br:12]Br.[Br:14][CH:15]1[CH2:21][CH2:20][C:19]2[CH:22]=[CH:23][CH:24]=[CH:25][C:18]=2[NH:17][C:16]1=[O:26]>C(O)(=O)C>[Br:14][CH:15]1[CH2:21][CH2:20][C:19]2[CH:22]=[C:23]([Br:12])[CH:24]=[CH:25][C:18]=2[NH:17][C:16]1=[O:26]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24408BromineHCID 5765032,3,4,5-tetrahydro-1H-1-benzazepineHCID 27571843-Bromo-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

생성물 1

HCID 588572193,7-dibromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Scheme 5 describes an example of bromination of a tetrahydrobenzazepine intermediate. Bromine can be added slowly to commercially available 3-bromo-1,3,4,5-tetrahydro-1-benzazepin-2-one in acetic acid with stirring at room temperature to provide the useful intermediate 3,7-dibromo-1,3,4,5-tetrahydro-1-benzazepin-2-one, which can be used in many transformations described herein. Bromination using similar conditions can be carried out on other amino aryl cores described herein to provide intermediates for transformation to the compounds of the invention described in Schemes 8, 9 and 10.

출처 및 근거

ORD 기록
ord-5dc8d1a4d7a64005aaa34528a13933b9
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07741317B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트