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Water → 4-[(S)-3-[(R)-1-(naphthalen-1-yl)ethylamino]pyrrolidin-1-yl]phenylethylsulfone

HRID 1811633
ノート
印刷プレビュー

反応式

HRID 1811633 の反応式
Cl.Cl.[C:3]1([C@H:13]([NH:15][C@H:16]2[CH2:20][CH2:19][NH:18][CH2:17]2)[CH3:14])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=1.F[C:22]1[CH:27]=[CH:26][C:25]([CH2:28][CH2:29][S:30]([CH2:33][CH2:34][C:35]2[CH:40]=[CH:39][C:38](F)=[CH:37][CH:36]=2)(=[O:32])=[O:31])=[CH:24][CH:23]=1.C(=O)([O-])[O-].[K+].[K+].O>CS(C)=O.C(Cl)(Cl)Cl>[C:3]1([C@H:13]([NH:15][C@H:16]2[CH2:20][CH2:19][N:18]([C:22]3[CH:27]=[CH:26][C:25]([CH2:28][CH2:29][S:30]([CH2:33][CH2:34][C:35]4[CH:40]=[CH:39][C:38]([N:18]5[CH2:19][CH2:20][C@H:16]([NH:15][C@@H:13]([C:3]6[C:12]7[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=7)[CH:6]=[CH:5][CH:4]=6)[CH3:14])[CH2:17]5)=[CH:37][CH:36]=4)(=[O:32])=[O:31])=[CH:24][CH:23]=3)[CH2:17]2)[CH3:14])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=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

7

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 534437264-FluorophenylethylsulfoneHCID 67408696(S)-3-[(R)-1-(naphthalen-1-yl)ethylamino]pyrrolidine dihydrochloride

生成物 1

HCID 674070244-[(S)-3-[(R)-1-(naphthalen-1-yl)ethylamino]pyrrolidin-1-yl]phenylethylsulfone収率 73.7%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒
HCID 6212Chloroform溶媒

反応条件

温度
130 °C

実験手順

To a solution of 150 mg of (S)-3-[(R)-1-(naphthalen-1-yl)ethylamino]pyrrolidine dihydrochloride and 108 mg of 4-fluorophenylethylsulfone in 2 ml of DMSO was added 263 mg of potassium carbonate, and the reaction mixture was stirred at 130° C. for 1 day. To the reaction mixture was added water and chloroform, the mixture was stirred and the liquids were separated. The organic layer was dried and evaporated, and then, the residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=80:20→40:60) to obtain 132.5 mg of 4-[(S)-3-[(R)-1-(naphthalen-1-yl)ethylamino]pyrrolidin-1-yl]phenylethylsulfone.

後処理

  1. stirringthe mixture was stirred
  2. customthe liquids were separated
  3. customThe organic layer was dried
  4. customevaporated
  5. customthe residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=80:20→40:60)

出典と根拠

ORDレコード
ord-fa54a85ba8734cb3b1c5902e5f364a86
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08362274B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート