Reacción #6980

ord-998102171ea145578b3da40483685ff2

Ecuación de reacción

O=C(O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid
O=C(O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
compound 52A
O=C(O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
NCC(F)(F)CN
2,2-difluoro-1,3-propanediamine
CCN(C(C)C)C(C)C
DIPEA
NCC(F)(F)CNC(=O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
title compound
Rendimiento 65.0%
NCC(F)(F)CNC(=O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
N-(3-Amino-2,2-difluoro-propyl)-4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzamide
Rendimiento 65.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with brine
  2. 2
    Secadodried over Na2SO4
  3. 3
    Concentraciónconcentrated
  4. 4
    OtroThe residue was purified by flash column chromatography [silica gel, 5% (NH3/MeOH(2M) in EtOAc]

Procedimiento

To a mixture of 4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid (compound 52A, 21 mg, 0.06 mmol) and HATU (38 mg, 0.1 mmol) in DMF (0.2 ml) and THF (0.4 ml), were added 2,2-difluoro-1,3-propanediamine (ref. Tetrahedron, 8617, 1994) (60 mg, 0.54 mmol) and DIPEA (26 mg, 0.2 mmol). The resulting mixture was stirred at RT for 18 h, then diluted with CH2Cl2, washed with brine, dried over Na2SO4 and concentrated. The residue was purified by flash column chromatography [silica gel, 5% (NH3/MeOH(2M) in EtOAc] to afford the title compound (17 mg, 65%) as a white solid. LC/MS; (M+H)+=437.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084160B2uspto-grants-2006_08