Hydrochloric Acid → 2-(3-Chloro-5-fluorophenyl)-5-pentylpyrimidine

HRID 2268712노트

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HRID 2268712 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([Mg]Br)[CH:5]=[C:6]([F:8])[CH:7]=1.ClC1C=C(Br)C=C(F)C=1.[Mg].Cl[C:22]1[N:27]=[CH:26][C:25]([CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:24][N:23]=1.Cl>C(OCC)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:22]2[N:23]=[CH:24][C:25]([CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:26][N:27]=2)[CH:5]=[C:6]([F:8])[CH:7]=1

참가 물질

7

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온도
-60 °C

실험 절차

A solution of 3-chloro-5-fluorophenylmagnesium bromide [prepared from 22.7 g (108.3 mmol) of 3-chloro-5-fluoro-bromobenzene and 2.7 g (111.0 mmol) of magnesium, and 100 ml of diethyl ether] in diethyl ether was added by drops to a mixture of 10 g (54.1 mmol) of 2-chloro-5-pentylpyrimidine, 0.4 g (0.5 mmol) of dichloro[1,1′-bis(diphenylphosphino) ferrrocene]palladium, and 300 ml of diethyl ether while being maintained at a temperature lower than −60° C., stirred at the same temperature for 1 hour, and then stirred at 10° C. for 10 hours. A diluted hydrochloric acid in an amount of 300 ml was added to the reaction mixture and extracted with 250 ml of heptane. The organic layer thus obtained was washed with a diluted aqueous sodium bicarbonate solution thrice and water thrice, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure and the residue was subjected to silica gel column chromatography (eluent: heptane/toluene=1/1) to obtain 11.0 g of a crude 2-(3-chloro-5-fluorophenyl)-5-pentylpyrimidine. (Yield: 72.8%)

후처리

  1. stirringstirred at 10° C. for 10 hours
  2. extractionextracted with 250 ml of heptane
  3. customThe organic layer thus obtained
  4. washwas washed with a diluted aqueous sodium bicarbonate solution thrice and water thrice
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off under a reduced pressure

출처 및 근거

ORD 기록
ord-5c99b135cf264570a5f6fc5e5a77e261
출처 데이터셋
uspto-grants-2001_12
특허 번호
US06329027B1

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