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N-Phenyl-p-phenylenediamine → 2,3,3a,4,5,9b-Hexahydro-4-(3-hydroxypropyl)-8-phenylamino-furano[3,2-c]quinoline

HRID 1297162
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HRID 1297162 반응식
[C:1]1([NH:7][C:8]2[CH:14]=[CH:13][C:11]([NH2:12])=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O[CH:16]1[CH2:20][CH2:19][CH2:18][O:17]1>O>[OH:17][CH2:16][CH2:20][CH2:19][CH:18]1[CH:19]2[CH2:20][CH2:16][O:17][CH:18]2[C:13]2[CH:14]=[C:8]([NH:7][C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[CH:9]=[CH:10][C:11]=2[NH:12]1
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참가 물질

4

반응물 2

HCID 7564N-Phenyl-p-phenylenediamineHCID 93002Tetrahydro-2-hydroxyfuran

생성물 1

HCID 589145972,3,3a,4,5,9b-Hexahydro-4-(3-hydroxypropyl)-8-phenylamino-furano[3,2-c]quinoline수율 86%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

The mixture of 4-(N-phenylamino)-aniline (2 mmol), 2-hydroxy-tetrahydrofuran (6 mmol) and InCl3 (0.2-0.4 mmol) in water (5 mL) was stirred at room temperature. The reaction was monitored by TLC. After 24 h stirring at room temperature, the reaction mixture was extracted with ethyl ether (3×20 mL). Removal of solvent and flash column chromatography gave 1,2,3,4-tetrahydroquinoline derivatives in 86% yield (cis:trans=46:54).

후처리

  1. stirringAfter 24 h stirring at room temperature
  2. extractionthe reaction mixture was extracted with ethyl ether (3×20 mL)
  3. customRemoval of solvent and flash column chromatography

출처 및 근거

ORD 기록
ord-5fbdcdb6119e4f449b16b7b82ec26342
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07250423B2

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