Cyanuric chloride → HCID 86636520, compound

HRID 2094579Notes

Reaction equation

HRID 2094579 reaction equation
[N:1]1[C:8]([Cl:9])=[N:7][C:5](Cl)=[N:4][C:2]=1[Cl:3].Cl.O.[NH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][C:13]1=O.C(=O)([O-])[OH:20].[Na+]>CC(C)=O.O>[Cl:9][C:8]1[N:1]=[C:2]([Cl:3])[N:4]=[C:5]([N:12]2[CH2:17][CH2:16][C:15](=[O:20])[CH2:14][CH2:13]2)[N:7]=1

Participants

6

Reactant 3

HCID 7954Cyanuric chlorideHCID 516892Sodium BicarbonateHCID 22021827Piperidone monohydrate hydrochloride

Product 1

HCID 86636520HCID 86636520, compound

Reagents, catalysts & solvents 2

HCID 180AcetoneSolvent2×HCID 962WaterSolvent2×

Conditions

Temperature
0 °C

Procedure

To magnetically stirred ice-water (72 mL) was added a solution of cyanuric chloride (2.2 g, 12 mmol) in acetone (48 mL), followed by piperidone monohydrate hydrochloride (1.8 g, 12 mmol) as a suspension in acetone (20 mL) and water (10 mL). To the mixture was added a suspension of sodium hydrogen carbonate (2.2 g, 24 mmol) in water (25 mL). The mixture was stirred at 0° C. for two hours. The title compound was collected by filtration, washed with water, and dried under vacuum.

Workup

  1. additionTo the mixture was added
  2. filtrationThe title compound was collected by filtration
  3. washwashed with water
  4. customdried under vacuum

Sources & evidence

ORD record
ord-9a3931cb7b924bbbbf1c281ecc7f5d5d
Source dataset
uspto-grants-2013_05
Patent number
US08445486B2

Reaction notes

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