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Water → 2-Methylsulfanyl-4-(5-methylsulfanyl-pyridin-2-yl)-6-trifluoromethyl-pyrimidine

HRID 1767707
ノート
印刷プレビュー

反応式

HRID 1767707 の反応式
[F:1][C:2]([F:17])([F:16])[C:3](=O)[CH2:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([S:13][CH3:14])=[CH:9][N:8]=1)=O.S(O)(O)(=O)=O.[CH3:23][S:24][C:25](=[NH:27])[NH2:26].C([O-])(=O)C.[Na+].O>C(O)(=O)C>[CH3:23][S:24][C:25]1[N:27]=[C:5]([C:7]2[CH:12]=[CH:11][C:10]([S:13][CH3:14])=[CH:9][N:8]=2)[CH:4]=[C:3]([C:2]([F:17])([F:16])[F:1])[N:26]=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

6

反応物 4

HCID 962WaterHCID 752702-Methyl-2-thiopseudourea sulfateHCID 517045Sodium AcetateHCID 17967065HCID 17967065、化合物

生成物 1

HCID 179670662-Methylsulfanyl-4-(5-methylsulfanyl-pyridin-2-yl)-6-trifluoromethyl-pyrimidine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
120 °C

実験手順

To a solution of 4,4,4-trifluoro-1-(5-methylsulfanyl-pyridin-2-yl)-butane-1,3-dione (0.600 g, 2.28 mmol) in glacial acetic acid (6 mL) was added 2-methyl 2-thiopseudourea sulphate (0.761 g, 2.74 mmol) and sodium acetate (0.224 g, 2.74 mmol). The reaction was heated to 120° C. under nitrogen for 21 hours. The reaction was allowed to cool before the addition of water (10 mL), leading to precipitation of a solid. The reaction mixture was poured onto water (10 mL) and stirred for 15 minutes at 22° C. The precipitate was filtered from the aqueous solution, washed with water, and dried in vacuo to yield the title compound as a grey solid: MS m/z 317 (M+1).

後処理

  1. customleading to precipitation of a solid
  2. additionThe reaction mixture was poured onto water (10 mL)
  3. filtrationThe precipitate was filtered from the aqueous solution
  4. washwashed with water
  5. customdried in vacuo

出典と根拠

ORDレコード
ord-0d8abb85d6774d678a8cde75fcc15953
出典データセット
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07235560B2

反応ノート

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