Methanol → 6-chloro-3-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)-pyrimidin-4(3H)-one

HRID 2059865

반응식

HRID 2059865 반응식
[Cl:1][C:2]1[N:7]=[CH:6][NH:5][C:4](=[O:8])[CH:3]=1.[OH:9][C:10]([CH3:25])([CH3:24])[CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16](B(O)O)=[CH:15][C:14]=1[O:22][CH3:23].N1C=CC=CC=1.CO>C(Cl)Cl>[Cl:1][C:2]1[N:7]=[CH:6][N:5]([C:16]2[CH:17]=[CH:18][C:13]([O:12][CH2:11][C:10]([OH:9])([CH3:25])[CH3:24])=[C:14]([O:22][CH3:23])[CH:15]=2)[C:4](=[O:8])[CH:3]=1

참가 물질

6

반응물 4

HCID 887MethanolHCID 1049Pyridine2회HCID 585798634-(2-Hydroxy-2-methylpropoxy)-3-methoxyphenylboronic acidHCID 1354454786-Chloropyrimidin-4-ol

생성물 1

HCID 585799166-chloro-3-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)-pyrimidin-4(3H)-one수율 46%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A mixture of 6-chloropyrimidin-4(3H)-one (50 mg, 0.383 mmol), 4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenylboronic acid Part D of Procedure 4 (184 mg, 0.766 mmol), copper (II) acetate, monohydrate (84 mg, 0.421 mmol), and pyridine (1.5 mL, 19.15 mmol) in DCM (4 mL) was stirred at RT under the presence of air overnight (21 hours). Pyridine (0.5 mL) and MeOH (0.5 mL) were added and continued to stir for 2 hours. The reaction was diluted with DCM, washed with 1N HCl, sat NaHCO3, dried (Na2SO4), and concentrated to afford crude product. The crude was purified using ISCO flash chromatography (silica gel/hexanes-ethyl acetate 100:0 to 0:100 gradient) to afford the desired product 6-chloro-3-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)-pyrimidin-4(3H)-one 11A (57.4 mg, 0.177 mmol, 46% yield) as a light brown solid.

후처리

  1. stirringto stir for 2 hours
  2. washwashed with 1N HCl
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. customto afford crude product
  6. customThe crude was purified

출처 및 근거

ORD 기록
ord-7602434f60244de98cdf58296eda172c
출처 데이터셋
uspto-grants-2012_10
특허 번호
US08278316B2

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