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1,1'-Carbonyldiimidazole → trans-1-[(3,4-Dichlorophenyl)acetyl]-2-(1-pyrrolidinylmethyl)-3-piperidinol hydrochloride

HRID 1196514
ノート
印刷プレビュー

反応式

HRID 1196514 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=O)[CH:5]=[CH:6][C:7]=1[Cl:8].C(N1C=CN=C1)(N1C=CN=C1)=O.[N:25]1([CH2:30][CH:31]2[CH:36]([OH:37])[CH2:35][CH2:34][CH2:33][NH:32]2)[CH2:29][CH2:28][CH2:27][CH2:26]1>O1CCCC1>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([N:32]2[CH2:33][CH2:34][CH2:35][C@@H:36]([OH:37])[C@@H:31]2[CH2:30][N:25]2[CH2:26][CH2:27][CH2:28][CH2:29]2)=[O:12])[CH:5]=[CH:6][C:7]=1[Cl:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 682631,1'-CarbonyldiimidazoleHCID 798743,4-Dichlorophenylacetic acidHCID 151232362-(Pyrrolidin-1-yl)methyl-3-hydroxy piperidine

生成物 1

HCID 67916857trans-1-[(3,4-Dichlorophenyl)acetyl]-2-(1-pyrrolidinylmethyl)-3-piperidinol hydrochloride

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 3,4-dichlorophenylacetic acid (4.45 g) and 1,1'-carbonyldiimidazole (4.16 g) in dry tetrahydrofuran (60 ml) was stirred at room temperature for 20 min before adding a solution of the product of stage (i) (4.0 g, 60:40 mixture of trans:cis isomers) in dry tetrahydrofuran. This solution was stirred for 16 h under nitrogen and concentrated in vacuo. Column chromatography of the residue on UGI alumina (10 cm diameter, 20 cm length) with graded elution from dichloromethane to dichloromethane:methanol (9:1) removed polar material. The mixture obtained was converted to the hydrochloride salt and crystallised from ethyl acetate:methanol (1:2). The mother liquors were concentrated and the residue was crystallised from the same solvent. The mother liquors from this second recrystallisation gave the title compound upon concentration as an amorphous solid (2.8 g), m.p. 115°-120°, which contained a 93:7 mixture of trans:cis isomers by h.p.l.c.

後処理

  1. concentrationconcentrated in vacuo
  2. washColumn chromatography of the residue on UGI alumina (10 cm diameter, 20 cm length) with graded elution from dichloromethane to dichloromethane:methanol (9:1)
  3. customremoved polar material
  4. customThe mixture obtained
  5. customcrystallised from ethyl acetate:methanol (1:2)
  6. concentrationThe mother liquors were concentrated
  7. customthe residue was crystallised from the same solvent
  8. customThe mother liquors from this second recrystallisation

出典と根拠

ORDレコード
ord-2afb34cc8e024fe3a821b6ab88c5c280
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05114945

反応ノート

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