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Potassium Carbonate → 2-Isopropyl-5,6-dihydro-1H-benzo[d]imidazol-7(4H)-one

HRID 1946521
ノート
印刷プレビュー

反応式

HRID 1946521 の反応式
Br[C:2]1[C:3](=O)[CH2:4][CH2:5][CH2:6][C:7]=1[O:8]CC.Cl.[CH3:13][CH:14]([CH3:18])[C:15](=[NH:17])[NH2:16].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:13][CH:14]([C:15]1[NH:17][C:3]2[CH2:4][CH2:5][CH2:6][C:7](=[O:8])[C:2]=2[N:16]=1)[CH3:18]
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

5

反応物 3

HCID 11430Potassium CarbonateHCID 27820532-Methylpropanimidamide hydrochlorideHCID 113334562-Bromo-3-ethoxy-2-cyclohexen-1-one

生成物 1

HCID 584601782-Isopropyl-5,6-dihydro-1H-benzo[d]imidazol-7(4H)-one収率 45%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

To 2-bromo-3-(ethyloxy)-2-cyclohexen-1-one (38.8 g) in a 1 L round-bottom flask in N,N-Dimethylformamide (DMF) (500 mL) was added 2-methylpropanimidamide hydrochloride (26.1 g) and potassium carbonate (61.2 g). The suspension was then stirred at 80° C. under nitrogen for 2 h. The mixture was filtered and as much DMF as possible was evaporated off under high vacuum. The sample was loaded in dichloromethane and purified by column chromatography over silica using a 0-30% methanol-dichloromethane gradient. The appropriate fractions were combined and evaporated in vacuo to give the required product 14.2 g as a brown solid. LC/MS MH+ 179, Rt 1.4 min (5 min run).

後処理

  1. filtrationThe mixture was filtered and as much DMF
  2. customas possible was evaporated off under high vacuum
  3. custompurified by column chromatography over silica using a 0-30% methanol-dichloromethane gradient
  4. customevaporated in vacuo

出典と根拠

ORDレコード
ord-f4dea2f51049433fa090e9340e9a3f37
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399444B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート