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Phosphorus oxychloride → HCID 18327906, 화합물

HRID 1250303
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HRID 1250303 반응식
[C:1]([O:5][C:6]([N:8]1[CH:13]=[CH:12][C:11](O)([C:14]2[N:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[CH:10]=[CH:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].P(Cl)(Cl)(Cl)=O>N1C=CC=CC=1>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11]([C:14]2[N:15]=[CH:16][CH:17]=[CH:18][N:19]=2)=[CH:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 18328032HCID 18328032, 화합물

생성물 1

HCID 18327906HCID 18327906, 화합물수율 51%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2.11 g of the compound of step 1 of Example 25 was dissolved in 30 ml of pyridine, then 1.0 ml (1.4 equivalents) of phosphorus oxychloride was added under ice cooling and the result was agitated for 15 hours. The pyridine was distilled off under reduced pressure, an aqueous solution of 10% sodium hydroxide was added and extraction was performed by methylene chloride. The organic layer was washed with saturated saline and was dried by anhydrous magnesium sulfate, then the solvent was distilled off and the resultant crude product was refined with silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain the above-referenced compound in an amount of 1.01 g (yield of 51%).

후처리

  1. distillationThe pyridine was distilled off under reduced pressure
  2. additionan aqueous solution of 10% sodium hydroxide was added
  3. extractionextraction
  4. washThe organic layer was washed with saturated saline
  5. dry with materialwas dried by anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off
  7. customto obtain the above-referenced compound in an amount of 1.01 g (yield of 51%)

출처 및 근거

ORD 기록
ord-b6c8df10395e43e1be627324484d5cb5
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06337397B1

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