Triethylamine → HCID 66969799, 화합물

HRID 1510299노트

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HRID 1510299 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([O:12][C@@H:13]([CH3:17])[CH2:14][O:15][CH3:16])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[F:18][C:19]1[CH:24]=[CH:23][C:22](B(O)O)=[CH:21][CH:20]=1.C(N(CC)CC)C>ClCCl.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:16][O:15][CH2:14][C@H:13]([CH3:17])[O:12][C:10]1[CH:9]=[C:4]([CH:3]=[C:2]([O:1][C:22]2[CH:23]=[CH:24][C:19]([F:18])=[CH:20][CH:21]=2)[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]

참가 물질

6

실험 절차

A suspension of methyl 3-hydroxy-5-[(1S)-2-methoxy-(1-methylethyl)oxy]benzoate (3.53 g, 14.7 mmol), p-fluoro-phenyl-boronic acid (16.2 mmol), copper(II) acetate (2.94 g, 16.2 mmol), triethylamine (10.3 ml, 73.5 mmol) and freshly activated 4A molecular sieves (17.7 g) in dichloromethane was stirred at ambient temperature and under ambient atmosphere for 2 days. The reaction mixture was filtered, and the dichloromethane was removed in vacuo. The residual oil was partitioned between ethyl acetate and 2 mol/l hydrochloric acid. The ethyl acetate layer was separated, washed with aqueous sodium hydrogen carbonate and brine, dried over Na2SO4 and evaporated to give a residue, which was purified by column chromatograph on silica gel (20-60% ethyl acetate in iso-hexane, gradient) to give the desired ester.

후처리

  1. filtrationThe reaction mixture was filtered
  2. customthe dichloromethane was removed in vacuo
  3. customThe residual oil was partitioned between ethyl acetate and 2 mol/l hydrochloric acid
  4. customThe ethyl acetate layer was separated
  5. washwashed with aqueous sodium hydrogen carbonate and brine
  6. dry with materialdried over Na2SO4
  7. customevaporated
  8. customto give a residue, which
  9. customwas purified by column chromatograph on silica gel (20-60% ethyl acetate in iso-hexane, gradient)

출처 및 근거

ORD 기록
ord-9853352328fb4e0690e5f6ca34b7b9d5
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08211925B2

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