Reaktion #2445752

ord-535a2e8eb44a41d0b006704194915e49

Reaktionsgleichung

Clc1ccc2c(Cl)ccnc2n1
product
Clc1ccc2c(Cl)ccnc2n1
2,5-Dichloro-[1,8]naphthyridine
CC(=O)Nc1ccc(Sc2ccc(C)cc2N)cc1
product
CC(=O)Nc1ccc(Sc2ccc(C)cc2N)cc1
N-[4-(2-Amino-4-methyl-phenylsulfanyl)-phenyl]-acetamide
→
CC(=O)Nc1ccc(Sc2ccc(C)cc2Nc2ccnc3nc(Cl)ccc23)cc1
title compound
Ausbeute 48.0%
CC(=O)Nc1ccc(Sc2ccc(C)cc2Nc2ccnc3nc(Cl)ccc23)cc1
N-{4-[2-(7-Chloro-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenyl}-acetamide
Ausbeute 48.0%

Edukte

Clc1ccc2c(Cl)ccnc2n1
product
Clc1ccc2c(Cl)ccnc2n1
2,5-Dichloro-[1,8]naphthyridine
CC(=O)Nc1ccc(Sc2ccc(C)cc2N)cc1
product
CC(=O)Nc1ccc(Sc2ccc(C)cc2N)cc1
N-[4-(2-Amino-4-methyl-phenylsulfanyl)-phenyl]-acetamide

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigegiving a crude solid
  2. 2
    Sonstigethat was purified by HPLC with TFA

Vorschrift

The product from Example 13d (200 mg, 1.0 mmol) and the product from Example 18b (215 mg, 1.0 mmol) were reacted following the procedure from Example 1g giving a crude solid that was purified by HPLC with TFA to give the title compound 200 mg, 48%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07763731B2uspto-grants-2010_07