Methylamine → N-(2'-Cyanobiphenyl-4-yl)methyl-N-methyl amine

HRID 1450394Notes

Reaction equation

HRID 1450394 reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]#[N:16])=[CH:5][CH:4]=1.[CH3:17][NH2:18]>C1COCC1>[C:15]([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[C:6]1[CH:7]=[CH:8][C:3]([CH2:2][NH:18][CH3:17])=[CH:4][CH:5]=1)#[N:16]

Participants

4

Reactant 2

HCID 6329MethylamineHCID 15019124'-(Bromomethyl)-2-cyanobiphenyl

Product 1

HCID 15337416N-(2'-Cyanobiphenyl-4-yl)methyl-N-methyl amine

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

62.1 g (228 mmol) 4-bromomethyl-2'-cyanobiphenyl (prepared according to . D. J. Carini et al., J. Med. Chem. 1992, 34, 2525) were dissolved in 3 l THF. After addition of 1.5 l of a 40% aqueous solution of methylamine the mixture was stirred over night at room temperature, and the THF distilled off in vacuo. The remaining aqueous layer was extracted with ethyl acetate, the extract dried by stirring over night with 0.4 nm mole sieve, and evaporated in vacuo. The title compound was obtained as a viscous oil, which was pure enough according to its 1H-NMR spectrum for further conversions,

Workup

  1. distillationthe THF distilled off in vacuo
  2. extractionThe remaining aqueous layer was extracted with ethyl acetate
  3. customthe extract dried
  4. stirringby stirring over night with 0.4 nm mole sieve
  5. customevaporated in vacuo

Sources & evidence

ORD record
ord-6a9e6fe04c0a4974865b88cd8ad5c016
Source dataset
uspto-grants-1997_02
Patent number
US05602136

Reaction notes

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