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Phenol → 1-(4-Pyridinylamino)-2-pyrrolidinone

HRID 981965
ノート
印刷プレビュー

反応式

HRID 981965 の反応式
[NH2:1][N:2]1[CH2:6][CH2:5][CH2:4][C:3]1=[O:7].C1(O)C=CC=CC=1.Cl.Br[C:17]1[CH:22]=[CH:21][N:20]=[CH:19][CH:18]=1>>[N:20]1[CH:21]=[CH:22][C:17]([NH:1][N:2]2[CH2:6][CH2:5][CH2:4][C:3]2=[O:7])=[CH:18][CH:19]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 996PhenolHCID 881004-Bromopyridinium chlorideHCID 124949741-Aminopyrrolidin-2-one

生成物 1

HCID 200687911-(4-Pyridinylamino)-2-pyrrolidinone収率 16%

反応条件

温度
140 °C

実験手順

A slurry consisting of 1-amino-2-pyrrolidinone (7.40 g), phenol (17.8 g), and 4-bromopyridine hydrochloride (15.8 g) was heated in a 140° C. oil bath for 70 minutes under nitrogen. The resulting solution was cooled to room temperature and purified via flash column chromatography (silica gel, 2% Et3N/0-50% MeOH/EtOAc) and preparative high performance liquid chromatography (HPLC) (silica gel, 10% MeOH/DCM). The resulting product fractions were concentrated and the product was redissolved in dichloromethane and sat. aqueous sodium bicarbonate. Exhaustive extraction of the aqueous layer afforded the pure product (free of triethyl amine salts). Recrystallization from dichloromethane/ether afforded 2.10 g (16%) of 1-(4-pyridinylamino)-2-pyrrolidinone, m.p. 177°-179.5° C.

後処理

  1. temperatureThe resulting solution was cooled to room temperature
  2. custompurified via flash column chromatography (silica gel, 2% Et3N/0-50% MeOH/EtOAc) and preparative high performance liquid chromatography (HPLC) (silica gel, 10% MeOH/DCM)
  3. concentrationThe resulting product fractions were concentrated
  4. dissolutionthe product was redissolved in dichloromethane
  5. extractionExhaustive extraction of the aqueous layer
  6. customafforded the pure product (free of triethyl amine salts)
  7. customRecrystallization from dichloromethane/ether

出典と根拠

ORDレコード
ord-9db8f35db0754207acb027988432eb80
出典データセット
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04994472

反応ノート

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