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3-(Trifluoromethyl)phenyl isocyanate → 1-(5-Bromopyridin-2-yl)-3-(3-(trifluoromethyl)phenyl)urea

HRID 1446747
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인쇄 미리보기

반응식

HRID 1446747 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH2:8])=[N:6][CH:7]=1.[F:9][C:10]([F:21])([F:20])[C:11]1[CH:12]=[C:13]([N:17]=[C:18]=[O:19])[CH:14]=[CH:15][CH:16]=1>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:18]([NH:17][C:13]2[CH:14]=[CH:15][CH:16]=[C:11]([C:10]([F:9])([F:20])[F:21])[CH:12]=2)=[O:19])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 94833-(Trifluoromethyl)phenyl isocyanateHCID 706222-Amino-5-bromopyridine

생성물 1

HCID 606503781-(5-Bromopyridin-2-yl)-3-(3-(trifluoromethyl)phenyl)urea수율 73%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5-bromopyridin-2-yl amine (1.190 g, 6.88 mmol, 1.0 eq.) in THF (20 mL), add 3-trifluoromethylphenyl isocyanate (0.96 mL, 6.88 mmol, 1.0 eq.) in a drop-wise manner at room temperature. Stir the reaction mixture at room temperature for 30 minutes. Filter the solid and wash with MeOH (2×10 mL). Dry the solid to afford 1.81 g (5.0 mmol, 73%) of the title compound. MS (ES), m/z 360, 362 (M+1).

후처리

  1. filtrationFilter the solid
  2. washwash with MeOH (2×10 mL)
  3. customDry the solid

출처 및 근거

ORD 기록
ord-bc742a9ac60145c5ae3820ec6fb8cdde
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666879B2

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