Reacción #324359

ord-fd0c4243253a42aca4db30ba11b3a6d1

Ecuación de reacción

O=C(Cl)c1cccc(C(=O)Cl)n1
2,6-pyridinedicarbonyl dichloride
NCc1c2ccccc2c(CN)c2ccccc12
9,10-bis(aminomethyl)anthracene
CCN(CC)CC
triethylamine
CO
methanol
c1ccc2cc3ccccc3cc2c1
Anthracene

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONthe mixture containing rotaxane 13 and polymer co-products
  2. 2
    Filtraciónwas filtered
  3. 3
    Lavadowashed with chloroform (100 mL)
  4. 4
    Extracciónto extract rotaxane 13
  5. 5
    Concentraciónthe filtrate was concentrated
  6. 6
    OtroPurification of the crude material by column chromatography
  7. 7
    Otrogave the rotaxane 13

Procedimiento

Clear solutions of 2,6-pyridinedicarbonyl dichloride (84 mg, 0.41 mmol) in 15 mL of chloroform and 9,10-bis(aminomethyl)anthracene (97 mg, 0.41 mmol) in 15 mL of chloroform were simultaneously added dropwise over 10 h to a stirred solution of squaraine 13a (32 mg, 0.05 mmol, synthesized according to E. Arunkumar et al. Chem. Eur. J. 2006, 12, 4884-4690) and triethylamine (81 mg, 0.8 mmol) in 30 mL of chloroform. After overnight stirring, the mixture containing rotaxane 13 and polymer co-products was filtered, washed with chloroform (100 mL) to extract rotaxane 13, and the filtrate was concentrated. Purification of the crude material by column chromatography using silica gel (gradient, 0-1% of MeOH in CHCl3) gave the rotaxane 13. λmax (abs): 651 m, λmax (em): 707 nm, 59% (methanol); λmax (abs): 648 nm, λmax (em): 700 nm, Q.Y.: 65% (chloroform).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08642014B2uspto-grants-2014_02