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Phosphorus oxybromide → 2,6-Dibromopyrido[3,2-d]pyrimidine

HRID 1799579
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HRID 1799579 반응식
P(Br)(Br)([Br:3])=O.[Br:6][C:7]1[N:8]=[CH:9][C:10]2[N:16]=[C:15](O)[CH:14]=[CH:13][C:11]=2[N:12]=1>CN(C)C=O>[Br:6][C:7]1[N:8]=[CH:9][C:10]2[N:16]=[C:15]([Br:3])[CH:14]=[CH:13][C:11]=2[N:12]=1
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참가 물질

4

반응물 2

HCID 24613Phosphorus oxybromideHCID 178515741HCID 178515741, 화합물

생성물 1

HCID 582166532,6-Dibromopyrido[3,2-d]pyrimidine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
90 °C

실험 절차

A roundbottom flask was charged with N,N-dimethylformamide (4.2 L). Phosphorus oxybromide (646.9 g, 2.26 mol, 2.30 equiv) was added followed by dropwise addition of 2-bromopyrido-[3,2-d]-pyrimidin-6-ol (170 g, 752.1 mmol). The resulting solution was allowed to react, with stirring, for 1 minute while the temperature was maintained at 90° C. The reaction mixture was then quenched by the addition of 10 L of water/ice. The resulting solution was extracted once with ethyl acetate. The organic layer was washed with aqueous NaHSO4 and brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was purified via silica gel chromatography eluting with dichloromethane to afford the title compound.

후처리

  1. customto react
  2. customThe reaction mixture was then quenched by the addition of 10 L of water/ice
  3. extractionThe resulting solution was extracted once with ethyl acetate
  4. washThe organic layer was washed with aqueous NaHSO4 and brine
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting residue was purified via silica gel chromatography
  9. washeluting with dichloromethane

출처 및 근거

ORD 기록
ord-579b20a13c7043d8a2376b614c34b18b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08344144B2

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