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2,6-Diethylaniline → 8-Amino-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

HRID 81972
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HRID 81972 반응식
C[Si](C)(C)[N-][Si](C)(C)C.[Na+].[CH2:11]([C:13]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][CH3:21])[C:14]=1[NH2:15])[CH3:12].[NH2:22][C:23]1[N:32]=[CH:31][C:30]2[CH2:29][CH2:28][C:27]3[C:33]([C:37](OCC)=[O:38])=[N:34][N:35]([CH3:36])[C:26]=3[C:25]=2[N:24]=1>C1COCC1>[NH2:22][C:23]1[N:32]=[CH:31][C:30]2[CH2:29][CH2:28][C:27]3[C:33]([C:37]([NH:15][C:14]4[C:16]([CH2:20][CH3:21])=[CH:17][CH:18]=[CH:19][C:13]=4[CH2:11][CH3:12])=[O:38])=[N:34][N:35]([CH3:36])[C:26]=3[C:25]=2[N:24]=1
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참가 물질

5

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HCID 113692,6-DiethylanilineHCID 2724254Sodium bis(trimethylsilyl)amideHCID 24993827ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

생성물 1

HCID 670756638-Amino-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide수율 80%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

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온도
0 °C

실험 절차

Sodium hexamethyldisilazide (NaHMDS) in THF (1.0 M, 11.0 mL, 11.0 mmol) was added over 30 min to a solution of 2,6-diethylaniline (1.2 mL, 8.32 mmol) and ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (0.760 g, 2.77 mmol) in THF (30 mL) at 0° C. The resulting brown solution was stirred at 0° C. for 10 min and allowed to warm to room temperature over a period of 30 min. After stirring at room temperature for 3 h, the reaction was quenched by the addiction of saturated acquesous NH4Cl (10 mL). The reaction was partitioned between ethyl acetate (50 mL) and water (50 mL). The acqueos layer was extracted with ethyl acetate (2×30 mL). The combined organic solution was washed with brine (50 mL), dried over Na2SO4, filtered and evaporated to dryness, the crude solid was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95/5) to afford 0.830 g (80% yield) of the title compound.

후처리

  1. temperatureto warm to room temperature over a period of 30 min
  2. stirringAfter stirring at room temperature for 3 h
  3. customthe reaction was quenched by the addiction of saturated acquesous NH4Cl (10 mL)
  4. customThe reaction was partitioned between ethyl acetate (50 mL) and water (50 mL)
  5. extractionThe acqueos layer was extracted with ethyl acetate (2×30 mL)
  6. washThe combined organic solution was washed with brine (50 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customevaporated to dryness
  10. customthe crude solid was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95/5)

출처 및 근거

ORD 기록
ord-597af241cbeb408ea88761810cd93bdf
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846701B2

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