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Cyclopentanol → Methyl 5-bromo-6-(cyclopentyloxy)nicotinate

HRID 1766436
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HRID 1766436 반응식
[CH:1]1([OH:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Na+].[CH3:9][O:10][C:11]([C:13]1[CH:14]=[N:15][C:16](Cl)=[C:17]([Br:19])[CH:18]=1)=[O:12]>CN(C=O)C>[CH3:9][O:10][C:11]([C:13]1[CH:14]=[N:15][C:16]([O:6][CH:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)=[C:17]([Br:19])[CH:18]=1)=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7298CyclopentanolHCID 24758Sodium hydrideHCID 2764313Methyl 5-bromo-6-chloronicotinate

생성물 1

HCID 66844699Methyl 5-bromo-6-(cyclopentyloxy)nicotinate수율 16%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Cyclopentanol (1 mL, 11 mmol) was dissolved in DMF (25 mL) and a dispersion of sodium hydride in oil (55–65%, 480 mg) was added at room temperature. The mixture was stirred for 1 h at room temperature and 5-bromo-6-chloro-3-pyridinecarboxylic acid methyl ester (2.5 g, 10 mmol) was added. Stirring was continued for 1 h at room temperature and the mixture was afterwards partitioned between water and diethyl ether. Organic phases were pooled, dried with MgSO4 and the solvent was evaporated. The residue was purified by column chromatography on silica (n-heptane/ethyl acetate 9:1) to yield 0.48 g of the title compound as a colorless oil, MS (EI) 299.0, 301.0 (M)+.

후처리

  1. stirringStirring
  2. waitwas continued for 1 h at room temperature
  3. customthe mixture was afterwards partitioned between water and diethyl ether
  4. dry with materialdried with MgSO4
  5. customthe solvent was evaporated
  6. customThe residue was purified by column chromatography on silica (n-heptane/ethyl acetate 9:1)

출처 및 근거

ORD 기록
ord-2392f459054640d29675299769cf2dc7
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07229999B2

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