Reacción #1893417

ord-16a06a40570c43ab95fa819c4bcc2391

Ecuación de reacción

CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
NaBH(OAc)3
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4cccc(C=O)c4)cc23)CC1
3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamide
NCc1ccc(O)c(O)c1
4-(aminomethyl)-1,2-benzenediol
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4cccc(CNCc5ccc(O)c(O)c5)c4)cc23)CC1
title compound
Rendimiento 15.1%
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4cccc(CNCc5ccc(O)c(O)c5)c4)cc23)CC1
5-[3-({[(3,4-dihydroxyphenyl)methyl]amino}methyl)phenyl]-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide
Rendimiento 15.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe resulting mixture was shaken overnight at ambient temperature after which time the solvent
  2. 2
    Otrowas removed under reduced pressure
  3. 3
    OtroThe crude product was purified by reverse phase HPLC (water/CH3CN, 0.1% TFA 10-90%)

Procedimiento

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamide (50 mg, 0.114 mmol) in dichloroethane (2 mL) was added 4-(aminomethyl)-1,2-benzenediol (12.1 mg, 0.087 mmol). The reaction solution was stirred at ambient temperature for 10 min prior to addition of NaBH(OAc)3 (58 mg, 0.261 mmol). The resulting mixture was shaken overnight at ambient temperature after which time the solvent was removed under reduced pressure. The crude product was purified by reverse phase HPLC (water/CH3CN, 0.1% TFA 10-90%) to give the title compound (7.4 mg, 12%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08354406B2uspto-grants-2013_01