Guanidine Hydrochloride → HCID 135493693、化合物

HRID 1020758

反応式

HRID 1020758 の反応式
C([O:3][C:4](=O)[CH2:5][C:6]([CH:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)=O)C.Cl.[NH2:15][C:16]([NH2:18])=[NH:17].CC(C)([O-])C.[K+]>CO>[NH2:17][C:16]1[NH:18][C:4](=[O:3])[CH:5]=[C:6]([CH:8]2[CH2:12][CH2:11][CH2:10][CH2:9]2)[N:15]=1

参加物

5

反応条件

温度
60 °C

実験手順

To a solution of 3-cyclopentyl-3-oxo-propionic acid ethyl ester (5.0 g, 27.4 mmol) and guanidine hydrochloride (3.1 g, 33.0 mmol) in MeOH (50 mL) at 23° C. was added potassium tert-butoxide, portionwise (16.7 g. 149 mmol) over 15 min with vigorous stirring and the reaction warmed to 60° C. The reaction was cooled to room temperature (rt) and stirred overnight and the precipitated salt was removed by filtration. The solution was concentrated to approximately 10 mL then diluted with 10 mL of water and adjusted to pH=5 by the addition of 6.0 N HCl (6.1 mL). The resulting precipitate was filtered and dried via suction then vacuum to yield a white solid (4.3 g, 87%) that was used without further purification. 1H NMR (MeOD): 10.71-10.54 (m, 1H), 6.58-6.32 (m, 2H), 5.44-5.37 (m, 1H), 2.66 (p, J=8.1, 1H), 1.91-1.73 (m, 2H), 1.72-1.48 (m, 6H).

後処理

  1. temperatureThe reaction was cooled to room temperature (rt)
  2. stirringstirred overnight
  3. customthe precipitated salt was removed by filtration
  4. concentrationThe solution was concentrated to approximately 10 mL
  5. additionthen diluted with 10 mL of water
  6. additionadjusted to pH=5 by the addition of 6.0 N HCl (6.1 mL)
  7. filtrationThe resulting precipitate was filtered
  8. customdried via suction

出典と根拠

ORDレコード
ord-acdce82425e740b7bf5c627129baeddd
出典データセット
uspto-grants-2014_05
特許番号
US08716475B2

関連ノート

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