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

Acetic Acid → 5-(6-Bromoimidazo[1,2-a]pyridin-2-yl)-2-(trifluoromethyl)aniline

HRID 539759
노트
인쇄 미리보기

반응식

HRID 539759 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[C:13]([N+:21]([O-])=O)[CH:12]=3)[N:10]=2)[CH:7]=1.CC(O)=O>[Fe].C(O)C.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([C:17]([F:19])([F:18])[F:20])=[C:13]([NH2:21])[CH:12]=3)[N:10]=2)[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 679827116-Bromo-2-[3-nitro-4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridine

생성물 1

HCID 575162715-(6-Bromoimidazo[1,2-a]pyridin-2-yl)-2-(trifluoromethyl)aniline수율 81.2%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 19096565Water ethanol용매

반응 조건

온도
80 °C

실험 절차

Fe (0.447 g) is added to a mixture of 6-bromo-2-[3-nitro-4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridine (0.618 g), HOAc (0.733 mL), and EtOH—H2O (10 mL, 4:1). The mixture is stirred at 80° C. for 2 hours, then concentrated, taken into sat. aqueous NaHCO3 and extracted with EtOAc and CH2Cl2. Organics are dried and concentrated to give the title compound (463 mg), which is used without further purification. LCMS m/z=356.4 [M+H]+, tR=2.04 min.

후처리

  1. concentrationconcentrated
  2. extractionextracted with EtOAc and CH2Cl2
  3. customOrganics are dried
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9d36e7de0956449e8384b29e2f64eb86
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871767B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트