Decylamine → HCID 70546760, compound

HRID 2059100Notes

Reaction equation

HRID 2059100 reaction equation
[OH:1][CH:2]([CH:26]1[CH2:31][C:30]([CH3:33])([CH3:32])[NH:29][C:28]([CH3:35])([CH3:34])[CH2:27]1)[CH2:3][NH:4][C:5]1[N:10]=[C:9]([NH:11][CH2:12][CH:13]([CH:15]2[CH2:20][C:19]([CH3:22])([CH3:21])[NH:18][C:17]([CH3:24])([CH3:23])[CH2:16]2)[OH:14])[N:8]=[C:7](Cl)[N:6]=1.[CH2:36]([NH2:46])[CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45].C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[OH:1][CH:2]([CH:26]1[CH2:31][C:30]([CH3:33])([CH3:32])[NH:29][C:28]([CH3:35])([CH3:34])[CH2:27]1)[CH2:3][NH:4][C:5]1[N:10]=[C:9]([NH:11][CH2:12][CH:13]([CH:15]2[CH2:20][C:19]([CH3:22])([CH3:21])[NH:18][C:17]([CH3:24])([CH3:23])[CH2:16]2)[OH:14])[N:8]=[C:7]([NH:46][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45])[N:6]=1

Participants

5

Reactant 3

HCID 8916DecylamineHCID 11430Potassium CarbonateHCID 867383042,4-Bis{2-hydroxy-N-(2,2,6,6-tetramethyl-4-piperidyl)ethylamino}-6-chloro-1,3,5-triazine

Product 1

HCID 70546760HCID 70546760, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Procedure

2,4-Bis{2-hydroxy-N-(2,2,6,6-tetramethyl-4-piperidyl)ethylamino}-6-chloro-1,3,5-triazine (3.0 g) and n-decylamine (1.5 g) were dissolved in dioxane (70 ml), followed by addition of potassium carbonate (1.0 g). The mixture was refluxed for 5 hours with stirring. After completion of the reaction, dioxane was distilled off and the resulting residue was recrystallized from ligroin to give the desired product as white crystals melting at 106°-107° C.

Workup

  1. temperatureThe mixture was refluxed for 5 hours
  2. distillationwas distilled off
  3. customthe resulting residue was recrystallized from ligroin

Sources & evidence

ORD record
ord-ec1b425e473548019b1cfff97b5211b0
Source dataset
uspto-grants-1982_03
Patent number
US04321374

Reaction notes

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