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Aniline → HCID 13568664, 화합물

HRID 231103
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인쇄 미리보기

반응식

HRID 231103 반응식
O1[CH2:6][CH2:5][N:4]([C:7]([C:9]2[CH:10]=[C:11]3[C:16](=[CH:17][CH:18]=2)[NH:15][C:14](=[O:19])[CH2:13][CH2:12]3)=[O:8])[CH2:3][CH2:2]1.[NH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:21]1([N:20]2[CH2:6][CH2:5][N:4]([C:7]([C:9]3[CH:10]=[C:11]4[C:16](=[CH:17][CH:18]=3)[NH:15][C:14](=[O:19])[CH2:13][CH2:12]4)=[O:8])[CH2:3][CH2:2]2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6115AnilineHCID 131953376-(Morpholine-4-carbonyl)-3,4-dihydroquinolin-2(1H)-one

생성물 1

HCID 13568664HCID 13568664, 화합물

실험 절차

2.62 Grams of 6-morpholinocarbonyl-3,4-dihydrocarbostyril and 10 g of aniline were placed in a sealed tube and heated at 170°-200° C. for 5 hours. Excess aniline was removed by evaporation under reduced pressure, then the residue thus obtained was purified by means of silica gel column chromatography. Recrystallized from isopropanol to obtain 0.32 g of 6-(4-phenyl-1-piperazinylcarbonyl)-3,4-dihydrocarbostyril. Colorless needle-like crystals. Melting point: 200°-201° C.

후처리

  1. temperatureheated at 170°-200° C. for 5 hours
  2. customExcess aniline was removed by evaporation under reduced pressure
  3. customthe residue thus obtained
  4. customwas purified by means of silica gel column chromatography
custom
Recrystallized from isopropanol

출처 및 근거

ORD 기록
ord-dc275cf8de2e483cba4ebe7baee714f0
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04845100

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