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Sodium Carbonate → ethyl 2-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylate

HRID 661489
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HRID 661489 반응식
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[CH2:15]([O:17][C:18]([C:20]1[C:21]([CH2:26][CH2:27][CH2:28][C:29]([OH:31])=O)=[CH:22][NH:23][C:24]=1[CH3:25])=[O:19])[CH3:16].C(=O)([O-])[O-].[Na+].[Na+]>>[CH3:25][C:24]1[NH:23][C:22]2[C:29](=[O:31])[CH2:28][CH2:27][CH2:26][C:21]=2[C:20]=1[C:18]([O:17][CH2:15][CH3:16])=[O:19]
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4

반응물 3

HCID 10340Sodium CarbonateHCID 14812Phosphorus oxide (P4O10)HCID 593760204-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acid

생성물 1

HCID 59376018ethyl 2-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylate수율 61%

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온도
70 °C

실험 절차

P2O5 7.1 g was added into polyphosphoric acid 142 g, then after the mixture was stirred for 30 minutes at 70° C., 4-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acid (S2) 6.3 g (0.026 mol) was added and stirred for 48 hours. The mixture was poured into the ice water and adjusted pH to 8 with saturated sodium carbonate solution, then extracted with ethyl acetate. The organic phase was washed with water and saturated sodium chloride solution, then dried over anhydrous Na2SO4 and concentrated to saturated solutions in vacuo. The residue was colded to −5° C., then the white solid was collected by filtration and dried in vacuum to give 3.5 g (61%) ethyl 2-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylate (S3).

후처리

  1. stirringstirred for 48 hours
  2. extractionextracted with ethyl acetate
  3. washThe organic phase was washed with water and saturated sodium chloride solution
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated to saturated solutions in vacuo
  6. customwas colded to −5° C.
  7. filtrationthe white solid was collected by filtration
  8. customdried in vacuum

출처 및 근거

ORD 기록
ord-fdf69f170d864b9d9c0014eece907c17
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084621B2

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