Реакция #1483039

ord-5521f83dc6c1418c8994ff382db94d86

Уравнение реакции

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
Выход 30.3%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe resulting reaction mixture
  2. 2
    ПромывкаThe organic layer was washed with saturated aqueous NaHCO3, brine
  3. 3
    Сушкаdried over Na2SO4
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated under reduced pressure
  6. 6
    ДругоеThe resulting residue was purified by silica gel chromatography (5% MeOH—CH2Cl2)

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE045275E1uspto-grants-2014_12