Pyridine → HCID 18543073, compound

HRID 1533213Notes

Reaction equation

HRID 1533213 reaction equation
[C:1]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:16][NH:17][C:18]([NH2:20])=[O:19].N1C=CC=CC=1>CO.O>[NH2:16][NH:17][C:18]([NH2:20])=[O:19].[C:1]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

6

Reactant 3

HCID 1049PyridineHCID 7170Ethyl benzoylacetateHCID 11236Semicarbazide hydrochloride

Product 1

HCID 18543073HCID 18543073, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Conditions

Temperature
-20 °C

Procedure

Ethyl benzoylacetate (5.0 g) is dissolved in methanol (10 mL) and added rapidly to a hot solution of semicarbazide hydrochloride (29 g) in water (130 mL). To this is added pyridine (4.1 g) and after heating to reflux for 5 minutes, the reaction mixture is cooled to −20° C. overnight. The resulting solid semicarbazone is collected by filtration, washed with water and then diethyl ether to give the desired product as white crystals.

Workup

  1. temperatureafter heating
  2. temperatureto reflux for 5 minutes
  3. filtrationThe resulting solid semicarbazone is collected by filtration
  4. washwashed with water

Sources & evidence

ORD record
ord-57346aed22c14e3bb5508caa121f1ec2
Source dataset
uspto-grants-2001_03
Patent number
US06207715B1

Reaction notes

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