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N,N'-Dimethylethylenediamine → 4-(4-chlorobenzylthio)-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyrimidin-2(1H)-one

HRID 2059844
ノート
印刷プレビュー

反応式

HRID 2059844 の反応式
CNCCNC.Br[C:8]1[CH:19]=[CH:18][C:11]([O:12][CH2:13][C:14]([CH3:17])([OH:16])[CH3:15])=[C:10]([O:20][CH3:21])[CH:9]=1.[Cl:22][C:23]1[CH:37]=[CH:36][C:26]([CH2:27][S:28][C:29]2[CH:34]=[CH:33][NH:32][C:31](=[O:35])[N:30]=2)=[CH:25][CH:24]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>O1CCOCC1.C(Cl)Cl.[Cu]I>[Cl:22][C:23]1[CH:37]=[CH:36][C:26]([CH2:27][S:28][C:29]2[CH:34]=[CH:33][N:32]([C:8]3[CH:19]=[CH:18][C:11]([O:12][CH2:13][C:14]([OH:16])([CH3:17])[CH3:15])=[C:10]([O:20][CH3:21])[CH:9]=3)[C:31](=[O:35])[N:30]=2)=[CH:25][CH:24]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 8070N,N'-DimethylethylenediamineHCID 62657Potassium Phosphate, TribasicHCID 595950491-(4-Bromo-2-methoxyphenoxy)-2-methylpropan-2-olHCID 1785185414-(4-chlorobenzylthio)pyrimidin-2(1H)-one

生成物 1

HCID 469268044-(4-chlorobenzylthio)-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyrimidin-2(1H)-one収率 7%

試薬・触媒・溶媒 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 6344Dichloromethane溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
105 °C

実験手順

N1,N2-dimethylethane-1,2-diamine (356 mg, 4.04 mmol) was added to a stirred mixture of 1-(4-bromo-2-methoxyphenoxy)-2-methylpropan-2-ol Part 1B of Procedure 1 (222 mg, 0.807 mmol), 4-(4-chlorobenzylthio)pyrimidin-2(1H)-one Part A (170 mg, 0.67 mmol), copper(I) iodide (77 mg, 0.404 mmol) and potassium phosphate, tribasic (857 mg, 4.04 mmol) in dioxane (8 mL). The mixture was stirred at 105° C. for 7 h. The reaction mixture was diluted with methylene chloride, washed with saturated sodium bicarbonate, dried (MgSO4) and concentrated. The crude product was subjected to ISCO flash chromatography (silica gel/hexane-EtOAc 100:0 to 0:100 gradient, used LC/MS to identify fractions containing the desired product) to afford the title compound 4-(4-chlorobenzylthio)-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyrimidin-2(1H)-one A-1 (22 mg, 0.048 mmol, 7% yield, eluted with 100% EtOAc) as a pale gummy solid.

後処理

  1. washwashed with saturated sodium bicarbonate
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated
  4. additioncontaining the desired product)

出典と根拠

ORDレコード
ord-b22015f9ca9643368105e36ca5acd36c
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08278316B2

反応ノート

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