Reacción #1483039

ord-5521f83dc6c1418c8994ff382db94d86

Ecuación de reacción

CN(CCN)CCNC(=O)OC(C)(C)C
tert-Butyl 2-((2-aminoethyl)(methyl)amino)ethylcarbamate
O=C(O)c1cccnc1
nicotinic acid
CCN=C=NCCCN(C)C
EDCI
CN(CCNC(=O)OC(C)(C)C)CCNC(=O)c1cccnc1
tert-butyl 2-(methyl(2-(nicotinamido)ethyl)amino)ethylcarbamate
Rendimiento 30.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe resulting reaction mixture
  2. 2
    LavadoThe organic layer was washed with saturated aqueous NaHCO3, brine
  3. 3
    Secadodried over Na2SO4
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated under reduced pressure
  6. 6
    OtroThe resulting residue was purified by silica gel chromatography (5% MeOH—CH2Cl2)

Procedimiento

tert-Butyl 2-((2-aminoethyl)(methyl)amino)ethylcarbamate (400 mg, 1.84 mmol) was taken up in CH3CN (10 mL) along with nicotinic acid (227 mg, 1.84 mmol) and EDCI (353 mg, 2.02 mmol). The resulting reaction mixture was stirred at room temperature for 18 h and then diluted with EtOAc. The organic layer was washed with saturated aqueous NaHCO3, brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (5% MeOH—CH2Cl2) to afford tert-butyl 2-(methyl(2-(nicotinamido)ethyl)amino)ethylcarbamate (180 mg, 30%). MS calculated for C16H26N4O3: 322.2. found: [M+H]+ 323.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE045275E1uspto-grants-2014_12