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HCID 22758819, 화합물 → HCID 22758848, 화합물

HRID 1704825
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HRID 1704825 반응식
C[O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][N:9]3[C:16](=[O:17])[C:15]([C:18]([O:20]CC)=[O:19])=[CH:14][N:13]=[C:10]32)=[CH:5][CH:4]=1>Br>[OH:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][N:9]3[C:16](=[O:17])[C:15]([C:18]([OH:20])=[O:19])=[CH:14][N:13]=[C:10]32)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 22758819HCID 22758819, 화합물

생성물 1

HCID 22758848HCID 22758848, 화합물수율 81%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

실험 절차

A solution of ethyl 6,7-dihydro-10-methoxy-4-oxo-4H-pyrimido[2,1-a]isoquinoline-3-carboxylate (5.0 g., 0.0175 mole) in 48% hydrobromic acid (125 ml.) was refluxed for 4 hours. The solution was cooled and the yellow product collected, washed with water, and dissolved in warm 0.5 N NaOH (80 ml.). The basic solution was treated with decolorizing carbon, filtered and the filtrate acidified with hydrochloric acid. The precipitated material was washed on the filter successively with water, ethanol and acetone to give 3.5 g. (81% yield) of the title acid, m.p. 326°-327°.

후처리

  1. temperatureThe solution was cooled
  2. customthe yellow product collected
  • washwashed with water
  • dissolutiondissolved in warm 0.5 N NaOH (80 ml.)
  • additionThe basic solution was treated with decolorizing carbon
  • filtrationfiltered
  • washThe precipitated material was washed on the
  • filtrationfilter successively with water, ethanol and acetone
  • customto give 3.5 g
  • 출처 및 근거

    ORD 기록
    ord-6fffbd6068e443cca6013c423c7d7d63
    출처 데이터셋
    uspto-grants-1978_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04127720

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