تفاعل #2317

ord-881c5d0cd109432183b9ebc50ee4284b

معادلة التفاعل

COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
product
COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]-phenoxyacetate
CN
methylamine
CNC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
title compound
CNC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
2-[4-[2-[4-(4-Pyridyl)piperazin-1-yl]acetyl]phenoxy]-N-methylacetamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solid formed
  2. 2
    ترشيحafter filtration
  3. 3
    غسيلwashing with a little ethyl acetate

الإجراء التجريبي

A suspension of the product of Example 1 (100 mg) in a 33% w/v solution of methylamine in ethanol (3 ml) was stirred for 18 hours. The solid formed, after filtration and washing with a little ethyl acetate, gave the title compound, 65 mg: m.p. 169°-171° C.; NMR (d6DMSO) δ 8.14 (2H, d), 8.06 (1H, bq), 8.00 (2H, d), 7.05 (2H, d), 6.80 (2H, d), 4.56 (2H, s), 3.82 (2H, s), 3.30 (4H, t), 2.66 (3H, d), 2.61 (4H, t); m/e 369 (M+H)+ ; calculated for C20H24N4O3 : C, 65.2; H, 6.6; N, 15.2. found: C, 65.0; H, 6.8; N, 15.1%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728701uspto-grants-1998_03