Reacción #2446057

ord-2cc6163a0a734a11a6984c56790720d4

Ecuación de reacción

CN1CCCC1=O
N-methylpyrrolidone
O=C1OC(=O)c2ccc(Cl)c3cccc1c23
6-chloro-1H,3H-benzo[de]isochromene-1,3-dione
Cl.NCCSSCCN
cystamine hydrochloride
CN1CCCC1=O
NMP
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
2,2′-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture is heated
  2. 2
    workup.STIRRINGwith stirring at 120° C. for 3 hours
  3. 3
    TemperaturaAfter cooling
  4. 4
    Otrothe precipitated product is recovered
  5. 5
    workup.ADDITIONthe filtered solution is extended by addition of 200 ml of water
  6. 6
    Otroa second precipitate is recovered
  7. 7
    LavadoThe precipitates are washed with water
  8. 8
    Otrodried
  9. 9
    Otro11.46 g of white powder are recovered

Procedimiento

9.30 g of 6-chloro-1H,3H-benzo[de]isochromene-1,3-dione and 4.46 g of hydrochlorided cystamine hydrochloride are suspended in 50 ml of N-methylpyrrolidone (NMP). 5.5 g of diisopropylethylamine are added and the mixture is heated with stirring at 120° C. After two hours, 50 ml of NMP are added and the mixture is kept with stirring at 120° C. for 3 hours. After cooling, the precipitated product is recovered and the filtered solution is extended by addition of 200 ml of water, and a second precipitate is recovered. The precipitates are washed with water and dried. 11.46 g of white powder are recovered. The analyses show that the product is in accordance with the expected product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08685114B2uspto-grants-2014_04