1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 17842642、化合物

HRID 459461ノート

反応式

HRID 459461 の反応式
O.ON1C2C=CC=C[C:6]=2N=N1.Cl.CN(C)CCCN=C=NCC.[N:24]1[CH:29]=[CH:28][C:27]([C:30]2[S:34][C:33]([C:35]([O-:37])=[O:36])=[N:32][CH:31]=2)=[CH:26][CH:25]=1.[Li+]>CO>[N:24]1[CH:29]=[CH:28][C:27]([C:30]2[S:34][C:33]([C:35]([O:37][CH3:6])=[O:36])=[N:32][CH:31]=2)=[CH:26][CH:25]=1

参加物

5

実験手順

1-Hydroxybenzotriazole monohydrate (805 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.71 g) were added to a solution of lithium 5-(4-pyridyl)thiazole-2-carboxylate (632 mg) in methanol (5.0 ml) at room temperature. After stirring for 4 days, the reaction mixture was concentrated under reduced pressure, and dichloromethane (20 ml), a saturated aqueous solution (100 ml) of sodium hydrogencarbonate and water (100 ml) were added to the residue to separate an organic layer. The water layer was then extracted with dichloromethane (2×20 ml). After the resultant organic layers were combined and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was then purified by column chromatography on silica gel (dichloromethane:acetone=5:1→2:1) to obtain the title compound (353 mg) as a colorless solid.

後処理

  1. concentrationthe reaction mixture was concentrated under reduced pressure, and dichloromethane (20 ml)
  2. additiona saturated aqueous solution (100 ml) of sodium hydrogencarbonate and water (100 ml) were added to the residue
  3. customto separate an organic layer
  4. extractionThe water layer was then extracted with dichloromethane (2×20 ml)
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe residue was then purified by column chromatography on silica gel (dichloromethane:acetone=5:1→2:1)

出典と根拠

ORDレコード
ord-6ff7152d71124235a52148445db50ece
出典データセット
uspto-grants-2007_03
特許番号
US07192968B2

反応ノート

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