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Triethylamine → HCID 54552519, 화합물

HRID 653121
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HRID 653121 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([C:14](=[O:17])[CH2:15][CH3:16])[CH2:9][CH2:8][C:7]2=[O:18])([O-:3])=[O:2].CO[CH:21](OC)[N:22]([CH3:24])[CH3:23].C(N(CC)CC)C>C1C=CC=CC=1>[CH3:21][N:22]([CH:24]=[C:8]1[C:7](=[O:18])[C:6]2[C:11](=[CH:12][CH:13]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[N:10]([C:14](=[O:17])[CH2:15][CH3:16])[CH2:9]1)[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 78373Dimethylformamide dimethyl acetalHCID 212947876-Nitro-4-oxo-1-propionyl1,2,3,4-tetrahydroquinoline

생성물 1

HCID 54552519HCID 54552519, 화합물수율 92%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A mixture of 6-nitro-4-oxo-1-propionyl-1,2,3,4tetrahydroquinoline (2.976 g), N,N-dimethylformamide dimethyl acetal (8.568 g), and triethylamine (1.818 g) in benzene (24 ml) was refluxed with stirring for 2.5 hours and cooled to room temperature. The resulting precipitates were collected by filtration, washed with cold ethyl acetate, and dried to give 3-dimethylaminomethylene-6-nitro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline (3.345 g).

후처리

  1. temperaturewas refluxed
  2. customThe resulting precipitates
  3. filtrationwere collected by filtration
  4. washwashed with cold ethyl acetate
  5. customdried

출처 및 근거

ORD 기록
ord-6a68e1b7f6da458c8ca6dce736a279c4
출처 데이터셋
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04675324

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