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Dimethylformamide → 1-Allyl-3-benzyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-one

HRID 501441
ノート
印刷プレビュー

反応式

HRID 501441 の反応式
C(=O)([O-])[O-].[K+].[K+].[CH2:7](Br)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.CN(C)C=O.[CH2:20]([N:23]1[C:31]2[CH:30]=[CH:29][N:28]=[C:27]([Cl:32])[C:26]=2[NH:25][C:24]1=[O:33])[CH:21]=[CH2:22]>C(OCC)(=O)C.O>[CH2:20]([N:23]1[C:31]2[CH:30]=[CH:29][N:28]=[C:27]([Cl:32])[C:26]=2[N:25]([CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:24]1=[O:33])[CH:21]=[CH2:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6228DimethylformamideHCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 230708521-Allyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-one

生成物 1

HCID 230705921-Allyl-3-benzyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-one収率 104.6%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

0.76 g of potassium carbonate and 0.94 g of benzyl bromide were added to a 50 ml N,N-dimethylformamide solution of 1.05 g of 1-allyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-one, and the mixture was stirred at room temperature for 14 hours. 300 ml of water and 300 ml of ethyl acetate were added to the solution, and the organic layer was washed three times with 100 ml of water and then with 100 ml of a saturated sodium chloride solution. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure to give 1.57 g of the title compound.

後処理

  1. washthe organic layer was washed three times with 100 ml of water
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-b173aea5a05a45b28bf6b2dd5d0453f7
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07772226B2

反応ノート

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