Guanidine Hydrochloride → HCID 135493693, compound

HRID 1020758

Reaction equation

HRID 1020758 reaction equation
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

Participants

5

Conditions

Temperature
60 °C

Procedure

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).

Workup

  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

Sources & evidence

ORD record
ord-acdce82425e740b7bf5c627129baeddd
Source dataset
uspto-grants-2014_05
Patent number
US08716475B2

Linked notes

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