반응 #480373

ord-3c51001c0d2447609ac10a00ff064941

반응 방정식

Clc1nc(SCc2ccccc2)nc2nc(Br)sc12
product
Clc1nc(SCc2ccccc2)nc2nc(Br)sc12
2-Bromo-7-chloro-5-[(phenylmethyl)thio]thiazolo[4,5-d]pyrimidine
NCCc1ccc(S(N)(=O)=O)cc1
4-(2-aminoethyl)benzenesulfonamide
CCN(C(C)C)C(C)C
N-ethyldiisopropylamine
NS(=O)(=O)c1ccc(CCNc2nc3nc(SCc4ccccc4)nc(Cl)c3s2)cc1
title compound
수율 78.4%
NS(=O)(=O)c1ccc(CCNc2nc3nc(SCc4ccccc4)nc(Cl)c3s2)cc1
4-[2-[[7-Chloro-5-[(phenylmethyl)thio]thiazolo[4,5-d]pyrimidin-2-yl]amino]ethyl]-benzenesulfonamide
수율 78.4%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The mixture was evaporated to dryness
  2. 2
    기타then purified (SiO2, ethyl acetate:dichloromethane 4:6 as eluant)

실험 절차

A solution of the product from Example 219 (0.3 g) in tetrahydrofuran (2 ml) containing 4-(2-aminoethyl)benzenesulfonamide (0.161 g) and N-ethyldiisopropylamine (0.5 ml) was stirred for 16 hours. The mixture was evaporated to dryness then purified (SiO2, ethyl acetate:dichloromethane 4:6 as eluant) to give the title compound (310 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06806273B1uspto-grants-2004_10