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Imidazole → 6,7-Dimethyl 5-methoxy-8-[[tris(1-methylethyl)silyl]oxy]-6,7-quinolinedicarboxylate

HRID 853693
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HRID 853693 반응식
N1C=CN=[CH:2]1.Cl[Si:7]([CH:14]([CH3:16])[CH3:15])([CH:11]([CH3:13])[CH3:12])[CH:8]([CH3:10])[CH3:9].[CH3:17][O:18][C:19]([C:21]1[C:22]([OH:36])=[C:23]2[C:28](=[C:29]([OH:35])[C:30]=1[C:31]([O:33][CH3:34])=[O:32])[N:27]=[CH:26][CH:25]=[CH:24]2)=[O:20].C([O-])([O-])=O.[K+].[K+].CI>CN(C=O)C>[CH3:17][O:18][C:19]([C:21]1[C:22]([O:36][CH3:2])=[C:23]2[C:28](=[C:29]([O:35][Si:7]([CH:14]([CH3:16])[CH3:15])([CH:11]([CH3:13])[CH3:12])[CH:8]([CH3:10])[CH3:9])[C:30]=1[C:31]([O:33][CH3:34])=[O:32])[N:27]=[CH:26][CH:25]=[CH:24]2)=[O:20]
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참가 물질

7

반응물 5

HCID 795ImidazoleHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 139400Triisopropylsilyl chlorideHCID 135742180Dimethyl 5,8-dihydroxy-6,7-quinolinedicarboxylate

생성물 1

HCID 589290076,7-Dimethyl 5-methoxy-8-[[tris(1-methylethyl)silyl]oxy]-6,7-quinolinedicarboxylate
수율 59%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

Imidazole (0.74 g, 10.8 mmol) and chlorotriisopropylsilane (TIPSCl, 1.15 g, 6.0 mmol) were added to 5,8-dihydroxy-quinoline-6,7-dicarboxylic acid dimethyl ester (prepared by the method in Oguchi, S. Bulletin of the Chemical Society of Japan 1974, 47, 1291, 1.5 g, 5.4 mmol) in 20 mL DMF. The reaction was stirred for 48 h at rt and then the reaction was partitioned between 0.5 L methyl t-butyl ether and 150 mL saturated aq. LiCl. The organic layer was dried over Na2SO4 and the solvent removed by rotary evaporation. The residue (1.4 g, 3.2 mmol) was redissolved in 25 mL DMF and treated with K2CO3 (0.66 g, 4.8 mmol) followed by methyl iodide (MeI, 0.6 g, 4.8 μL) at rt. After 2 h, the reaction mixture was concentrated and purified by introduction of the reaction mixture onto silica gel for flash chromatography (4/1 hexanes/ethyl acetate) to give 5-methoxy-8-triisopropylsilanyloxy-quinoline-6,7-dicarboxylic acid dimethyl ester (1.4 g, 59% overall yield): 1H NMR (CDCl3) δ 8.85 (d, 1H), 8.45 (d, 1H), 7.50 (dd, 1H), 4.05 (s, 3H), 3.95 (s, 3H), 3.90 (s, 3H), 1.45 (septet, 3H), 1.05 (d, 9H); MS: 448 (M+H).

후처리

  1. customprepared by the method in Oguchi, S
  2. customthe reaction was partitioned between 0.5 L methyl t-butyl ether and 150 mL saturated aq. LiCl
  3. dry with materialThe organic layer was dried over Na2SO4
  4. customthe solvent removed by rotary evaporation
  5. waitAfter 2 h
  6. concentrationthe reaction mixture was concentrated
  7. custompurified by introduction of the reaction mixture onto silica gel for flash chromatography (4/1 hexanes/ethyl acetate)

출처 및 근거

ORD 기록
ord-86e64417dfa641e6a1593160519a6d74
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07253180B2

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