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Stannous chloride dihydrate → HCID 19390586, 화합물

HRID 1756507
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HRID 1756507 반응식
[CH2:1]([O:4][C:5]([C:7]1[CH:16]=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[C:12]([N+:17]([O-])=O)[CH:13]=2)[N:8]=1)=[O:6])[CH:2]=[CH2:3].O.O.Cl[Sn]Cl>CO>[CH2:1]([O:4][C:5]([C:7]1[CH:16]=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[C:12]([NH2:17])[CH:13]=2)[N:8]=1)=[O:6])[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 19390567HCID 19390567, 화합물

생성물 1

HCID 19390586HCID 19390586, 화합물수율 28%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 2-allyloxycarbonyl-6-nitroquinoline (1.25 g; 4.8 mM) in MeOH (20 ml) was added SnCl2.2H2O (7.65 g, 33.6 mM). After stirring at ambient temperature for 3 hours, the mixture was evaporated to dryness and the residue partitioned between an aqueous solution of NH4OH (pH 8.5) and ethyl acetate. The organic phase was concentrated and purified by subjecting to flash chromatography, eluting with ethyl acetate/petroleum ether (65/35) to give 2-allyloxycarbonyl-6-aminoquinoline (280 mg; 28%).

후처리

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  1. customthe mixture was evaporated to dryness
  2. customthe residue partitioned between an aqueous solution of NH4OH (pH 8.5) and ethyl acetate
  3. concentrationThe organic phase was concentrated
  4. custompurified
  5. washeluting with ethyl acetate/petroleum ether (65/35)

출처 및 근거

ORD 기록
ord-260a0709056745d79a11cc38de02b69e
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05441949

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