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HCID 68704968, 화합물 → HCID 136388716, 화합물

HRID 61984
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HRID 61984 반응식
C[O:2][C:3]1[CH:4]=[C:5]([C:14]2[CH:19]=[CH:18][N:17]=[C:16]([C:20]3[C:21]([C:26]([F:29])([F:28])[F:27])=[N:22][CH:23]=[CH:24][CH:25]=3)[N:15]=2)[CH:6]=[C:7]([N+:11]([O-:13])=[O:12])[C:8]=1[O:9]C>Br>[N+:11]([C:7]1[CH:6]=[C:5]([C:14]2[CH:19]=[CH:18][N:17]=[C:16]([C:20]3[C:21]([C:26]([F:29])([F:28])[F:27])=[N:22][CH:23]=[CH:24][CH:25]=3)[N:15]=2)[CH:4]=[C:3]([OH:2])[C:8]=1[OH:9])([O-:13])=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 68704968HCID 68704968, 화합물

생성물 1

HCID 136388716HCID 136388716, 화합물

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

반응 조건

온도
140 °C

실험 절차

A suspension of 4-(3,4-dimethoxy-5-nitrophenyl)-2-(2-(trifluoromethyl)pyridin-3-yl)pyrimidine (0.239 g, 0.59 mmol) in 48% hydrobromic acid (5 mL) was stirred at 140° C. for four hours and then allowed to cool to room temperature. The mixture was poured onto ice-water (100 mL) and the resulting filtrate was filtered off, washed with water and dried to give 3-nitro-5-(2-(2-(trifluoromethyl)pyridin-3-yl)pyrimidin-4-yl)benzene-1,2-diol, 0.201 g (90%).

후처리

  1. temperature
to cool to room temperature
  • additionThe mixture was poured onto ice-water (100 mL)
  • filtrationthe resulting filtrate was filtered off
  • washwashed with water
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-c93f5dabbf96404e9b1837021c20b68b
    출처 데이터셋
    uspto-grants-2016_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09446012B2

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