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Potassium Carbonate → 8-Chloro-3,4-dihydro-1H-pyrimido[1,6-A]pyrimidin-6(2H)-one

HRID 920361
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HRID 920361 반응식
Br[CH2:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[C:10]([Cl:12])[N:9]=[C:8](Cl)[N:7]=1.C(=O)([O-])[O-:15].[K+].[K+]>O1CCOCC1.O>[Cl:12][C:10]1[CH:11]=[C:6]2[NH:5][CH2:4][CH2:3][CH2:2][N:7]2[C:8](=[O:15])[N:9]=1
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참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 86676391N-(3-bromopropyl)-2,6-dichloropyrimidin-4-amine

생성물 1

HCID 1357418828-Chloro-3,4-dihydro-1H-pyrimido[1,6-A]pyrimidin-6(2H)-one수율 55.5%

시약·촉매·용매 2

HCID 962Water용매HCID 312751,4-Dioxane용매

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온도
60 °C

실험 절차

A suspension of N-(3-bromopropyl)-2,6-dichloropyrimidin-4-amine (47 g, 165 mmol) and potassium carbonate (68.4 g, 495 mmol) in 1,4-dioxane (100 mL) and water (100 mL), was heated to 60° C. overnight. The mixture was evaporated to remove the dioxane solvent and the mixture was adjusted to pH ˜6 with HCl (6M). The mixture was extracted with ethyl acetate to remove by product and aqueous phase was adjusted to pH ˜7 with NaOH (2M), evaporated to afford the title compound (17 g, 55% yield).

후처리

  1. customThe mixture was evaporated
  2. customto remove the dioxane solvent
  3. extractionThe mixture was extracted with ethyl acetate
  4. customto remove by product and aqueous phase
  5. customevaporated

출처 및 근거

ORD 기록
ord-363685049e044985bc56aceed9d34aa9
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273054B2

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