Реакция #1605750

ord-6e11d24013f44838b42696f3069075d5

Уравнение реакции

O=C(Cl)c1ccc2c(c1)OCO2
benzo[1,3]dioxole-5-carbonyl chloride
CCCC(N)CCC
heptan-4-amine
CCN(CC)CC
triethylamine
CCCC(CCC)NC(=O)c1ccc2c(c1)OCO2
N-(heptan-4-yl)benzo[d][1,3]dioxole-5-carboxamide
Выход 48.5%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеSolvent was removed under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in EtOAc
  3. 3
    ПромывкаThe organic layer was washed successively with 1 N aq. HCl, 1 N aq. NaOH, water, brine
  4. 4
    Сушкаdried (MgSO4)
  5. 5
    Концентрированиеconcentrated
  6. 6
    ДругоеThe residue was recrystallized in EtOAc

Методика

To a solution of heptan-4-amine (8.06 mL, 54 mmol) in triethylamine (15.3 mL, 108 mmol) and dichloromethane (135 mL), was added, dropwise at 0° C., a solution of benzo[1,3]dioxole-5-carbonyl chloride (10 g, 54 mmol) dissolved in dichloromethane (135 mL). The reaction mixture was stirred for 1 h. Solvent was removed under reduced pressure and the residue was dissolved in EtOAc. The organic layer was washed successively with 1 N aq. HCl, 1 N aq. NaOH, water, brine, dried (MgSO4) and concentrated. The residue was recrystallized in EtOAc and Hexanes to afford 6.9 g of N-(heptan-4-yl)benzo[d][1,3]dioxole-5-carboxamide (48.3%) as a white solid. 1H NMR (500 MHz, CDCl3): δ 0.92 (t, 6H), 1.38 (m, 6H), 1.53 (m, 2H), 4.11 (m, 1H), 5.63 (m, 1H), 6.01 (s, 2H), 7.98 (d, 1H), 7.27 (s, d, 2H). MS (M+H, 264).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09072313B2uspto-grants-2015_07