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

Water → (6-Bromo-quinoxalin-2-yl)-(3-chloro-benzyl)-amine

HRID 1020734
노트
인쇄 미리보기

반응식

HRID 1020734 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7](Cl)[CH:6]=[N:5]2.[Cl:13][C:14]1[CH:15]=[C:16]([CH:19]=[CH:20][CH:21]=1)[CH2:17][NH2:18].O>CS(C)=O>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([NH:18][CH2:17][C:16]1[CH:19]=[CH:20][CH:21]=[C:14]([Cl:13])[CH:15]=1)[CH:6]=[N:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 77802Benzenemethanamine, 3-chloro-HCID 126864086-Bromo-2-chloroquinoxaline

생성물 1

HCID 66797253(6-Bromo-quinoxalin-2-yl)-(3-chloro-benzyl)-amine

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a solution of 6-Bromo-2-chloro-quinoxaline (0.3 g, 1 eq., 1.23 mmol) in DMSO (9 mL), was added 3-chloro benzyl amine (0.87 g, 5 eq., 6.2 mmol) at room temperature. The reaction mixture was stirred at room temperature overnight. After completion of the reaction, water (60 mL) was added and the reaction mixture was extracted with ethyl acetate (30 mL×3). The organic layer was washed with water (60 mL) and brine (60 mL), then dried over Na2SO4. The organic layer was concentrated under vacuum to obtain the crude product.

후처리

  1. additionwas added
  2. extractionthe reaction mixture was extracted with ethyl acetate (30 mL×3)
  3. washThe organic layer was washed with water (60 mL) and brine (60 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationThe organic layer was concentrated under vacuum

출처 및 근거

ORD 기록
ord-cbc5967b404645719c641b283b111c80
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716473B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트