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Ammonium Acetate → HCID 178469476, 화합물

HRID 745961
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HRID 745961 반응식
[CH3:1][O:2][C:3]([N:5]1[CH2:9][C:8](N2CCCC2)=[C:7]([C:15](=[O:26])[C:16]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:17][N:18](C)C)[CH2:6]1)=[O:4].C([O-])(=O)C.[NH4+]>C(O)C>[OH:26][C:15]1[C:16]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:17][N:18]=[C:8]2[CH2:9][N:5]([C:3]([O:2][CH3:1])=[O:4])[CH2:6][C:7]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 517165Ammonium AcetateHCID 53784406HCID 53784406, 화합물

생성물 1

HCID 178469476HCID 178469476, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 10.96 g of N-methoxycarbonyl-3-(2-ethoxycarbonyl-3-dimethylaminoacryloyl)-4-pyrrolidino-2,5-dihydropyrrole and 20 g of ammonium acetate in 250 ml of dry ethanol is refluxed for 90 minutes. The solution is cooled in an ice bath and the precipitate is filtered off to yield ethyl 4-hydroxy-5,7-dihydro-6-methoxycarbonylpyrrolo[3,4-b]pyridine-3-carboxylate, mp 274°-6°(dec); NMR (CF3COOD): 11.08 (s), 9.14 (s), 5.20 (s), 5.00 (s), 4.65 (q), 3.99 (s) and 1.52 (t).

후처리

  • temperatureThe solution is cooled in an ice bath
  • filtrationthe precipitate is filtered off
  • 출처 및 근거

    ORD 기록
    ord-6a3e250729ea4ae19cad140e7c0969d0
    출처 데이터셋
    uspto-grants-1986_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04602014

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