2-Chloro-4,6-diphenyl-1,3,5-triazine → HCID 66797655, compound

HRID 2275933Notes

Reaction equation

HRID 2275933 reaction equation
[CH3:1][C:2]1([CH3:22])[C:14]2[CH:13]=[C:12]3[NH:15][C:16]4[C:21]([C:11]3=[CH:10][C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2)=[CH:20][N:19]=[CH:18][CH:17]=4.[H-].[Na+].Cl[C:26]1[N:31]=[C:30]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[N:29]=[C:28]([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[N:27]=1>CN(C)C=O.C1COCC1>[C:38]1([C:28]2[N:29]=[C:30]([C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)[N:31]=[C:26]([N:15]3[C:12]4=[CH:13][C:14]5[C:2]([CH3:22])([CH3:1])[C:3]6[C:8]([C:9]=5[CH:10]=[C:11]4[C:21]4[C:16]3=[CH:17][CH:18]=[N:19][CH:20]=4)=[CH:7][CH:6]=[CH:5][CH:4]=6)[N:27]=2)[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1

Participants

6

Reactant 3

HCID 196982-Chloro-4,6-diphenyl-1,3,5-triazineHCID 24758Sodium hydrideHCID 66797983HCID 66797983, compound

Product 1

HCID 66797655HCID 66797655, compound

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 8028TetrahydrofuranSolvent

Procedure

10 g (35.17 mmol) of 10,10-dimethyl-10,12-dihydro-3,12-diazaindeno-[2,1-b]fluorene are dissolved in 150 ml of dimethylformamide under a protective-gas atmosphere, and 1.7 g of 60% NaH in mineral oil (42.2 mmol) are added. After 1 h at room temperature, a solution of 2-chloro-4,6-diphenyl-1,3,5-triazine (10.7 g, 38.68 mmol) in 100 ml of THF is added dropwise. The reaction mixture is stirred at room temperature for 12 h. After this time, the reaction mixture is poured onto ice and extracted three times with dichloromethane. The combined organic phases are dried over Na2SO4 and evaporated. The residue is extracted with hot toluene, recrystallised from toluene and finally sublimed in a high vacuum, the purity is 99.9%. The yield is 14.4 g (80%).

Workup

  1. additionare added
  2. additionAfter this time, the reaction mixture is poured onto ice
  3. extractionextracted three times with dichloromethane
  4. dry with materialThe combined organic phases are dried over Na2SO4
  5. customevaporated
  6. extractionThe residue is extracted with hot toluene
  7. customrecrystallised from toluene

Sources & evidence

ORD record
ord-f8fba96b669846a38dd9b1c1b36bdb47
Source dataset
uspto-grants-2015_09
Patent number
US09126970B2

Reaction notes

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