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Phosphorus oxybromide → 2-Bromobenzo[4,5]imidazo[1,2-a]pyrimidine

HRID 2361508
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반응식

HRID 2361508 반응식
P(Br)(Br)([Br:3])=O.[N:6]1[C:7]2[N:8]([C:13]3[CH:19]=[CH:18][CH:17]=[CH:16][C:14]=3[N:15]=2)[CH:9]=[CH:10][C:11]=1O>ClCCCl.CN(C=O)C>[Br:3][C:11]1[CH:10]=[CH:9][N:8]2[C:13]3[CH:19]=[CH:18][CH:17]=[CH:16][C:14]=3[N:15]=[C:7]2[N:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24613Phosphorus oxybromideHCID 178516346HCID 178516346, 화합물

생성물 1

HCID 583623562-Bromobenzo[4,5]imidazo[1,2-a]pyrimidine수율 100%

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매HCID 6228Dimethylformamide용매

반응 조건

온도
100 °C

실험 절차

Phosphorus oxybromide (25 g, 87 mmol) was added to a suspension of benzo[4,5]imidazo[1,2-a]pyrimidin-2-ol (5.2 g, 28.1 mmol) in DCE (Ratio: 1.000, Volume: 93 ml) and DMF (Ratio: 0.01, Volume: 0.927 ml). Heated the reaction mixture to 100° C. for 3 hours. Cooled the reaction to room temperature and concentrated. Diluted with ice water and quenched to pH ˜8 with concentrated ammonium hydroxide. The resulting residue was filtered and washed with water followed by ethyl ether. Dried under vacuum to afford crude 2-bromobenzo[4,5]imidazo[1,2-a]pyrimidine (6.97 g, 28.1 mmol, 100% yield).

후처리

  1. temperatureCooled
  2. customthe reaction to room temperature
  3. concentrationconcentrated
  4. additionDiluted with ice water
  5. customquenched to pH ˜8 with concentrated ammonium hydroxide
  6. filtrationThe resulting residue was filtered
  7. washwashed with water
  8. customDried under vacuum

출처 및 근거

ORD 기록
ord-14df6210e34a49649043685d60def443
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691187B2

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