Potassium Carbonate → 3-[(1S)-1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-5-ethynyl-2-pyridinamine

HRID 1845897노트

반응식

HRID 1845897 반응식
[Cl:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([Cl:9])[C:3]=1[C@@H:10]([O:12][C:13]1[C:14]([NH2:25])=[N:15][CH:16]=[C:17]([C:19]#[C:20][Si](C)(C)C)[CH:18]=1)[CH3:11].C(=O)([O-])[O-].[K+].[K+]>CO>[Cl:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([Cl:9])[C:3]=1[C@@H:10]([O:12][C:13]1[C:14]([NH2:25])=[N:15][CH:16]=[C:17]([C:19]#[CH:20])[CH:18]=1)[CH3:11]

참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 89708471HCID 89708471, 화합물

생성물 1

HCID 897084843-[(1S)-1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-5-ethynyl-2-pyridinamine수율 94.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

(S)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(2-(trimethylsilyl)ethynyl)-2-aminopyridine (10.6 g, 26.7 mmol) was dissolved in methanol (50 mL), potassium carbonate (7.38 g, 53.4 mmol) was added, and the reaction was stirred overnight at room temperature. TLC test showed that the raw materials were completely reacted. The reaction liquid was concentrated under reduced pressure, extracted with ethyl acetate; the organic layer was washed with water and saturated sodium chloride solution successively, dried over anhydrous sodium sulfate, concentrated; the residue was purified via silica gel column chromatography [petroleum ether:ethyl acetate=3:1 (v:v)] to yield the target product as yellow solid (8.2 g, yield: 94%).

후처리

  1. customwere completely reacted
  2. customThe reaction liquid
  3. concentrationwas concentrated under reduced pressure
  4. extractionextracted with ethyl acetate
  5. washthe organic layer was washed with water and saturated sodium chloride solution successively
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customthe residue was purified via silica gel column chromatography [petroleum ether:ethyl acetate=3:1 (v:v)]

출처 및 근거

ORD 기록
ord-7c16eb2099e545f586f3b258ba20ce47
출처 데이터셋
uspto-grants-2015_02
특허 번호
US08952002B2

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