تفاعل #2345

ord-bc4c5bfd0a2540ebba7d4dbbdd3411b3

معادلة التفاعل

COC(=O)C(CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1)NC(=O)OC(C)(C)C
compound
COC(=O)C(CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1)NC(=O)OC(C)(C)C
Methyl 2-t-butoxycarbonylamino-4-[4-[4-(4-pyridyl)-piperazin-1-yl]phenoxy]butyrat
COC(=O)C(N)CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
title compound
المردود 74.1%
COC(=O)C(N)CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Methyl 2-amino-4-[4-[4-(4-pyridyl) piperazin-1-yl]-phenoxy]butyrate
المردود 74.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solution was evaporated
  2. 2
    workup.DISSOLUTIONthe residue dissolved in water (15 ml)
  3. 3
    استخلاصThe mixture was extracted three times with dichloromethane
  4. 4
    أخرىEvaporation of the combined extracts

الإجراء التجريبي

The compound of Example 140 (0.96 g) in TFA (10 ml) was kept at room temperature for 2 hours. The solution was evaporated and the residue dissolved in water (15 ml) and the solution basified with sodium carbonate. The mixture was extracted three times with dichloromethane. Evaporation of the combined extracts gave the title compound (0.56 g); m.p. 125°-127° C.; NMR(d6DMSO) δ 8.2(2H,d), 6.92(6H,m), 4.0(2H,m), 3.64(3H,s), 3.46(4H,t), 3.15(4H,t), 2.04(2H,m), 1.84(1H, m); m/e 371(M+H)+. Calculated for C20H26N4 O3. 0.75 H2O: C, 62.5; H, 7.17; N, 14.6. Found: C, 62.8; H, 6.8; N, 14.3%.

المصدر

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