Sodium Hydroxide → 1-{4-[5-(2-Fluorobiphenyl-4-yl)-[1,2,4]oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid benzyl ester

HRID 2407486노트

반응식

HRID 2407486 반응식
[OH-].[Na+].[CH2:3]([O:10][C:11]([C:13]1([C:44]([O:46]CC2C=CC=CC=2)=[O:45])[CH2:18][CH2:17][N:16]([CH2:19][C:20]2[CH:25]=[CH:24][C:23]([C:26]3[N:30]=[C:29]([C:31]4[CH:36]=[CH:35][C:34]([C:37]5[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=5)=[C:33]([F:43])[CH:32]=4)[O:28][N:27]=3)=[CH:22][CH:21]=2)[CH2:15][CH2:14]1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>O1CCCC1>[CH2:3]([O:10][C:11]([C:13]1([C:44]([OH:46])=[O:45])[CH2:18][CH2:17][N:16]([CH2:19][C:20]2[CH:21]=[CH:22][C:23]([C:26]3[N:30]=[C:29]([C:31]4[CH:36]=[CH:35][C:34]([C:37]5[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=5)=[C:33]([F:43])[CH:32]=4)[O:28][N:27]=3)=[CH:24][CH:25]=2)[CH2:15][CH2:14]1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

참가 물질

4

실험 절차

An aqueous solution (50 mL) of sodium hydroxide (1.7 g, 0.043 mol) is added to a stirred solution of 1-{4-[5-(2-fluorobiphenyl-4-yl)-1,2,4-oxadiazole-3-yl]benzyl}piperidine-4,4-dicarboxylic acid dibenzyl ester (18.3 g, 0.027 mol) in tetrahydrofuran (150 mL). The reaction mixture is stirred overnight at room temperature and then concentrated under reduced pressure. The residue is acidified to pH ˜6 with diluted hydrochloric acid to give a solid which is filtered and washed with diethylether (100 mL) to furnish 1-{4-[5-(2-fluorobiphenyl-4-yl)-1,2,4-oxadiazole-3-yl]benzyl}piperidine-4,4-dicarboxylic acid mono benzyl ester.

후처리

  1. concentrationconcentrated under reduced pressure
  2. customto give a solid which
  3. filtrationis filtered
  4. washwashed with diethylether (100 mL)

출처 및 근거

ORD 기록
ord-acb151fcca0c40f389563bdf56a77f1c
출처 데이터셋
uspto-grants-2014_08
특허 번호
US08809539B2

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