تفاعل #2161264

ord-3a90672e12ef4b9ea8c3606f09635cb8

معادلة التفاعل

COC(=O)Cn1nc(-c2ccncc2)cc1Cc1ccc(F)cc1
Methyl [5-(4-fluorobenzyl)-3-pyridin-4-yl-1H-pyrazol-1-yl]acetate
C1CCOC1
THF
[Li+].[OH-]
LiOH
O=C(O)Cn1nc(-c2ccncc2)cc1Cc1ccc(F)cc1
title compound
المردود 93.7%
O=C(O)Cn1nc(-c2ccncc2)cc1Cc1ccc(F)cc1
[5-(4-fluorobenzyl)-3-pyridin-4-yl-1H-pyrazol-1-yl]acetic acid
المردود 93.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 12 liter, three-neck, round bottom flask equipped with mechanical stirrer
  2. 2
    أخرىthe majority of the THF was removed by rotary evaporation
  3. 3
    ترشيحthe white precipitate was filtered
  4. 4
    غسيلwashed with water
  5. 5
    أخرىAfter being dried under reduced pressure

الإجراء التجريبي

A 12 liter, three-neck, round bottom flask equipped with mechanical stirrer was charged with Methyl [5-(4-fluorobenzyl)-3-pyridin-4-yl-1H-pyrazol-1-yl]acetate (235 g, 0.72 mol), THF (3.5 L), methanol (1.2 L), and 2 M LiOH (1.2 L). The resulting solution was stirred at room temperature for 1.5 hours. After LC-MS showed the absence of starting material, the majority of the THF was removed by rotary evaporation. The solution was then acidified with 2 M HCl (pH=3) and the white precipitate was filtered and washed with water. After being dried under reduced pressure, 210 g (93%) of the title compound was obtained. 1H NMR (400 MHz, DMSO-D6) δ ppm 8.53 (d, 2 H), 7.68 (d, 2 H), 7.31 (t, 2 H), 7.14 (t, 2 H), 6.57 (s, 1 H), 5.00 (s, 2 H), 4.01 (s, 2 H); m/z (APCI+) for C17H14N3O2F 312.2 (M+H)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07919488B2uspto-grants-2011_04