4-(Dimethylamino)cyclohexan-1-one → HCID 131721938, compound

HRID 1870530Notes

Reaction equation

HRID 1870530 reaction equation
[Cl:1]CC1C=CC(NC(C2CCOC3C=CC(C4C=CC(C)=CC=4)=CC=3C=2)=O)=CC=1.C[N:31](C)[CH:32]1[CH2:37][CH2:36][C:35](=[O:38])[CH2:34][CH2:33]1>CN(C)C=O>[Cl-:1].[O:38]=[C:35]1[CH2:36][CH2:37][CH:32]([NH3+:31])[CH2:33][CH2:34]1

Participants

4

Reactant 2

HCID 103745454-(Dimethylamino)cyclohexan-1-oneHCID 18472316N-(4-chloromethylphenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide

Product 1

HCID 131721938HCID 131721938, compoundYield 384.6%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent2×

Procedure

To a solution of N-(4-chloromethylphenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (214 mg, 0.530 mmol) in N,N-dimethylformamide (1 ml) was dropwise added a solution of 4-dimethylaminocyclohexanone (112 mg, 0.795 mmol) in N,N-dimethylformamide (1 ml). Under nitrogen atmosphere, the mixture was stirred for 14 hours. The solvent was evaporated to give crude product, which was washed with ether to give N,N-dimethyl-N-(((7-(4-methylphenyl)-2,3-dihydro-1-benzoxepin-4-yl)carbonyl)amino)benzyl)-N-(4-oxocyclohexyl)ammonium chloride (Compound 2) (305 mg) as colorless powder.

Workup

  1. customThe solvent was evaporated
  2. customto give crude product, which
  3. washwas washed with ether

Sources & evidence

ORD record
ord-9dae5e8a3dbf4325bc23b49f450f0725
Source dataset
uspto-grants-2000_08
Patent number
US06096780

Reaction notes

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