Реакция #417942

ord-a76ba1f3b0ac456bb8cdf65b35c10a73

Уравнение реакции

CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C
bis(pinacolato)diboron
CC(=O)[O-].[K+]
potassium acetate
CCOC(=O)c1ccc(N)c(N)c1
bromide
CCOC(=O)c1ccc(N)c(N)c1
3,4-diamino-benzoic acid ethyl ester
COC(=O)c1ccc(B(O)O)cc1
2
COC(=O)c1ccc(B(O)O)cc1
4-methoxycarbonylphenylboronic acid

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ПромывкаThe organic phase was washed with H2O (20 mL)
  2. 2
    Сушкаdried over sodium sulfate
  3. 3
    Концентрированиеconcentrated in vacuo
  4. 4
    ДругоеThe residue was further purified by silica gel column chromatography (haxanes/ethyl acetate=1/4 to 0/1 (v/v))

Методика

Referring to Scheme 11-1, to a solution of the bromide 1 (2.0 g, 4.2 mmol, prepared according to published conditions) in dioxane (60 mL) was added bis(pinacolato)diboron (4.32 g, 17 mmol), Pd(PPh3)4 (0.49 g, 0.42 mmol) and potassium acetate (2.06 g, 21 mmol) under nitrogen atmosphere. The reaction mixture was stirred at 80° C. for 5 h, and then diluted with ethyl acetate (150 mL). The organic phase was washed with H2O (20 mL), dried over sodium sulfate and concentrated in vacuo. The residue was further purified by silica gel column chromatography (haxanes/ethyl acetate=1/4 to 0/1 (v/v)) to give 2 (1.73 g, 79% yield). LC-MS (ESI): m/z 523.3 (M+H)+.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08877707B2uspto-grants-2014_11