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Acetic Anhydride → HCID 12899518, 화합물

HRID 621567
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HRID 621567 반응식
[N:1]1([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:20]=[CH:19][CH:18]=[C:17]3[C:12]=2[CH2:13][CH2:14][C:15](=[O:21])[NH:16]3)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[C:22](OC(=O)C)(=[O:24])[CH3:23]>C(O)(=O)C>[C:22]([N:4]1[CH2:5][CH2:6][N:1]([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:20]=[CH:19][CH:18]=[C:17]3[C:12]=2[CH2:13][CH2:14][C:15](=[O:21])[NH:16]3)[CH2:2][CH2:3]1)(=[O:24])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 14128502HCID 14128502, 화합물

생성물 1

HCID 12899518HCID 12899518, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

20 grams of 5-(3-piperazinylpropoxy)-3,4-dihydrocarbostyril are mixed with 15 ml of acetic anhydride and 10 ml of acetic acid and heated for 5 hours under refluxing conditions. The reaction mixture is concentrated under reduced pressure to dryness. The residue is recrystallized from Ethanol to obtain 5-[3-(4-acetylpiperazinyl)propoxy]-3,4-dihydrocarbostyril in the form of colorless needle-like crystals with a melting point of 143°-145° C.

후처리

  1. temperature
heated for 5 hours under refluxing conditions
  • concentrationThe reaction mixture is concentrated under reduced pressure to dryness
  • customThe residue is recrystallized from Ethanol
  • 출처 및 근거

    ORD 기록
    ord-8fa58d99109b402cbc6407529d3f344a
    출처 데이터셋
    uspto-grants-1989_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04824840

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