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Chloranil → HCID 13338400, 화합물

HRID 2417687
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HRID 2417687 반응식
[CH3:1][N:2]1[C:6]2[C:7]3[N:8]([CH2:12][CH:13]([CH3:15])[N:14]=3)[C:9]([CH3:11])=[N:10][C:5]=2[C:4]([CH3:16])=[N:3]1.C1(Cl)C(=O)C(Cl)=C(Cl)C(=O)C=1Cl>C1(C)C(C)=CC=CC=1>[CH3:1][N:2]1[C:6]2[C:7]3[N:8]([CH:12]=[C:13]([CH3:15])[N:14]=3)[C:9]([CH3:11])=[N:10][C:5]=2[C:4]([CH3:16])=[N:3]1
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참가 물질

4

반응물 2

HCID 8371ChloranilHCID 13338380HCID 13338380, 화합물

생성물 1

HCID 13338400HCID 13338400, 화합물수율 50.7%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A mixture of 2.4 g (0.011 mol) of 7,8-dihydro-1,3,5,8-tetramethyl-1H-imidazo[1,2-c]pyrazolo[3,4-e]pyrimidine and 5.6 g (0.022 mol) of chloranil in 400 ml of xylene is stirred under reflux four hours. The warm mixture is extracted with two 150 ml portions of 1N sodium hydroxide. The organic layer is separated, filtered, dried over MgSO4, and evaporated in vacuo. The solid residue is stirred in ether to give 1.2 g (50%) of the title compound, mp 198°-200°.

후처리

  1. temperatureunder reflux four hours
  2. extractionThe warm mixture is extracted with two 150 ml portions of 1N sodium hydroxide
  3. customThe organic layer is separated
  4. filtrationfiltered
  5. dry with materialdried over MgSO4
  6. customevaporated in vacuo
  7. stirringThe solid residue is stirred in ether

출처 및 근거

ORD 기록
ord-0fdd88bbdf924c38ab59a019dacce00f
출처 데이터셋
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04469868

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