Hydrochloric Acid → Ethyl 2-(4-cyano-2-methoxyphenyl)-3-(dimethylamino)acrylate

HRID 526432노트

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HRID 526432 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([O:12][C:13]([CH3:16])(C)C)=[O:11])=[C:5]([O:17][CH3:18])[CH:4]=1)#[N:2].Cl.O1CCOCC1.C(C1C=CC(CC(OCC)=O)=C(OC)C=1)#N.C(O[CH:45](OCC)[N:46]([CH3:48])[CH3:47])C>C(O)C.CN(C=O)C.CCOC(C)=O>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9](=[CH:45][N:46]([CH3:48])[CH3:47])[C:10]([O:12][CH2:13][CH3:16])=[O:11])=[C:5]([O:17][CH3:18])[CH:4]=1)#[N:2]

참가 물질

9

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온도
100 °C

실험 절차

Combined tert-butyl 2-(4-cyano-2-methoxyphenyl)acetate (549 mg, 2.218 mmol) and 4N HCl in dioxane (0.277 mL, 1.109 mmol) in ethanol (7.4 mL) and stirred for 16 hours at 60° C. The reaction was concentrated by rotary evaporation and then combined with ethyl 2-(4-cyano-2-methoxyphenyl)acetate (0.486 g, 2.217 mmol) and 1,1-diethoxy-N,N-dimethylmethanamine (1.9 mL, 11.08 mmol) in DMF (4.43 mL) and stirred for 16 hours at 100° C. The reaction mixture was diluted with 200 mL EtOAc and washed twice with 200 mL water. Organic layer was dried with sodium sulfate and concentrated to give a residue which was purified on a 60 g NH silica gel column eluting with hexanes and EtOAc to give the title compound (405 mg, 74%).

후처리

  1. concentrationThe reaction was concentrated by rotary evaporation
  2. washwashed twice with 200 mL water
  3. dry with materialOrganic layer was dried with sodium sulfate
  4. concentrationconcentrated
  5. customto give a residue which
  6. customwas purified on a 60 g NH silica gel column
  7. washeluting with hexanes and EtOAc

출처 및 근거

ORD 기록
ord-8e16190dd5b04168948c0b4c0bd1e4ca
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09345713B2

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