تفاعل #1747857

ord-21ae7a7d8b3b47eeab4afbcfebdef308

معادلة التفاعل

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
المردود 82.1%
CN1c2ccc(-c3ccc4ccccc4c3)cc2Sc2cc(-c3ccc4ccccc4c3)ccc21
greenish-yellow solid
المردود 82.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحfiltered
  2. 2
    غسيلThe residue was washed with 470 ml of ethanol and hot water
  3. 3
    أخرىdried at 70° C. under reduced pressure
  4. 4
    workup.DISSOLUTIONThe solid was dissolved in 200 ml of methylene chloride
  5. 5
    ترشيحfiltered through silica gel
  6. 6
    أخرىAfter the solvent had been removed under reduced pressure

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08029919B2uspto-grants-2011_10