反应 #1747857

ord-21ae7a7d8b3b47eeab4afbcfebdef308

反应方程式

CN1c2ccc(Br)cc2Sc2cc(Br)ccc21
3,7-dibromo-10-methylphenothiazine
OB(O)c1ccc2ccccc2c1
2-naphthylboronic acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CN1c2ccc(-c3ccc4ccccc4c3)cc2Sc2cc(-c3ccc4ccccc4c3)ccc21
10-Methyl-3,7-bis(2-naphthyl)phenothiazine
收率 82.1%
CN1c2ccc(-c3ccc4ccccc4c3)cc2Sc2cc(-c3ccc4ccccc4c3)ccc21
greenish-yellow solid
收率 82.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤filtered
  2. 2
    洗涤The residue was washed with 470 ml of ethanol and hot water
  3. 3
    其他dried at 70° C. under reduced pressure
  4. 4
    workup.DISSOLUTIONThe solid was dissolved in 200 ml of methylene chloride
  5. 5
    过滤filtered through silica gel
  6. 6
    其他After the solvent had been removed under reduced pressure

实验过程

9.30 g (25.1 mmol) of 3,7-dibromo-10-methylphenothiazine, 9.50 g (55.2 mmol) of 2-naphthylboronic acid, 0.407 g (0.50 mmol) of bis(triphenylphosphine)palladium dichloride and 3.80 g (27.5 mmol) of potassium carbonate were heated to boiling under reflux under nitrogen for 5 hours in 204 ml of dimethoxyethane and 101 ml of water. The reaction mixture was cooled to room temperature, stirred further overnight and then filtered. The residue was washed with 470 ml of ethanol and hot water, and then dried at 70° C. under reduced pressure. The solid was dissolved in 200 ml of methylene chloride and filtered through silica gel. After the solvent had been removed under reduced pressure, 9.6 g of greenish-yellow solid were obtained (melting point 276-281° C.) and were recrystallized from 500 ml of toluene. 7.10 g (81% of theory) of analytically pure, shiny yellow microcrystals having a melting point of 285-289° C. were obtained, whose solution in chloroform fluoresced at λ=402 nm.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08029919B2uspto-grants-2011_10