Water → 4-(2-(2,6-Dimethyl-3-nitrophenoxy)pyridin-3-yl)pyrimidine

HRID 1361686

反応式

HRID 1361686 の反応式
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4]([CH3:11])[C:3]=1[OH:12].Cl[C:14]1[C:19]([C:20]2[CH:25]=[CH:24][N:23]=[CH:22][N:21]=2)=[CH:18][CH:17]=[CH:16][N:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+].O>CS(C)=O>[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4]([CH3:11])[C:3]=1[O:12][C:14]1[C:19]([C:20]2[CH:25]=[CH:24][N:23]=[CH:22][N:21]=2)=[CH:18][CH:17]=[CH:16][N:15]=1

参加物

6

反応物 4

HCID 962WaterHCID 10796Cesium carbonateHCID 814763-Nitro-2,6-xylenolHCID 161089744-(2-Chloropyridin-3-yl)pyrimidine

生成物 1

HCID 669706854-(2-(2,6-Dimethyl-3-nitrophenoxy)pyridin-3-yl)pyrimidine

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

Dissolved 2,6-dimethyl-3-nitrophenol (1.96 g, 11.7 mmol) and 4-(2-chloropyridin-3-yl)pyrimidine (1.50 g, 7.83 mmol) in dimethylsulfoxide (15.0 ml) and added cesium carbonate (5.10 g, 15.7 mmol). Reaction mixture was heated to 1200C in a sealed tube for 8 hours. Reaction mixture was then allowed to cool to room temperature and then poured into 250 mL of rapidly stirring water in an Erlenmeyer flask. After 10 minutes, the opaque brown aqueous solution was cooled to 0° C. and allowed to stand for 10 minutes, then filtered. The precipitate was collected as the title compound. MS m/z=323 (M+H)+. Calc'd for C17H16N4O3: 324.34.

後処理

  1. customReaction mixture
  2. customReaction mixture
  3. temperaturethe opaque brown aqueous solution was cooled to 0° C.
  4. waitto stand for 10 minutes
  5. filtrationfiltered
  6. customThe precipitate was collected as the title compound

出典と根拠

ORDレコード
ord-9896c3dafcf04df5a1785cc19e976847
出典データセット
uspto-grants-2011_02
特許番号
US07880000B2

関連ノート

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