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

N-bromobutanimide → 3-Bromo-5-(3-fluoropyridin-4-yl)-6-pyridin-3-ylpyrazin-2-amine

HRID 1710688
노트
인쇄 미리보기

반응식

HRID 1710688 반응식
[F:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[C:8]1[N:9]=[CH:10][C:11]([NH2:20])=[N:12][C:13]=1[C:14]1[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=1.[Br:21]N1C(=O)CCC1=O>CS(C)=O.O>[Br:21][C:10]1[C:11]([NH2:20])=[N:12][C:13]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)=[C:8]([C:7]2[CH:6]=[CH:5][N:4]=[CH:3][C:2]=2[F:1])[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 160708355-(3-Fluoropyridin-4-yl)-6-pyridin-3-ylpyrazin-2-amine

생성물 1

HCID 594576503-Bromo-5-(3-fluoropyridin-4-yl)-6-pyridin-3-ylpyrazin-2-amine수율 31%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매2회

실험 절차

To a 0° C. stirred solution of 5-(3-fluoropyridin-4-yl)-6-pyridin-3-ylpyrazin-2-amine (Example 115) (1.10 g, 4.11 mmol) in a mixture of DMSO (13 mL) and water (0.34 mL), was added N-bromosuccinimide (0.77 g, 4.32 mmol) in portions. After stirring for 5 h at room temperature, the mixture was poured into water, the precipitate collected by filtration, washed with water and dried to give the title compound as a green solid (0.44 g, 31%).

후처리

  1. filtrationthe precipitate collected by filtration
  2. washwashed with water
  3. customdried

출처 및 근거

ORD 기록
ord-0dc508299fd24ca8836ea461e1c9a048
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07790728B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트