Reacción #704363

ord-1a25b87a62d743c3ad64eaa5fa0c8dcd

Ecuación de reacción

Nc1nc(C2CCNCC2)c2ccccc2n1
2-amino-4-(4-piperidinyl)quinazoline
O=C(O)Cc1ccc(O)c(O)c1
3,4-dihydroxyphenylacetic acid
Nc1nc(C2CCN(C(=O)Cc3ccc(O)c(O)c3)CC2)c2ccccc2n1
titled compound
Rendimiento 60.2%
Nc1nc(C2CCN(C(=O)Cc3ccc(O)c(O)c3)CC2)c2ccccc2n1
2-amino-4-[1-(3,4-dihydroxyphenylacetyl)-4-piperidinyl]quinazoline
Rendimiento 60.2%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was removed in vacuo
  2. 2
    Otrothe residue was crystallized from methanol

Procedimiento

To an ice-cold solution of 2-amino-4-(4-piperidinyl)quinazoline (600 mg, 2.63 mmol) obtained in example 11(1), 3,4-dihydroxyphenylacetic acid (530 mg, 3.16 mmol) and 4-dimethylaminopyridine (386 mg, 3.16 mmol) in dimethylformamide (20 ml) was added 1-ethyl-3-(N,N'-dimethylaminopropyl)carbodiimide hydrochloride (605 mg, 3.16 mmol) under a nitrogen atmosphere. The mixture was stirred overnight at room temperature. The solvent was removed in vacuo and the residue was crystallized from methanol to give the titled compound (599 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05948786uspto-grants-1999_09