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(3R)-pyrrolidin-3-amine → cis-dichloro-(3R)-3-aminopyrrolidine platinum (II)

HRID 2165249
ノート
印刷プレビュー

反応式

HRID 2165249 の反応式
[NH2:1][C@@H:2]1[CH2:6][CH2:5][NH:4][CH2:3]1.[Cl-:7].[K+].[Pt+2:9].[Cl-:10].[Cl-]>O>[Pt+2:9].[Cl:7][C@@H:3]1[C@H:2]([NH2:1])[CH2:6][CH2:5][N:4]1[Cl:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1519352(3R)-pyrrolidin-3-amineHCID 86744074platinum (II) potassium chloride

生成物 1

HCID 18640044cis-dichloro-(3R)-3-aminopyrrolidine platinum (II)収率 78.7%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

(3R)-3-Aminopyrrolidine (400 mg) prepared in Reference Example 1-(3) is dissolved in water (200 ml) and thereto is added platinum (II) potassium chloride (2.0 g), and the mixture is stirred at room temperature for 20 hours. The precipitated solid is removed by filtration, and the filtrate is concentrated under reduced pressure. To the residue is added water (3 ml), and the resulting crystals are separated by filtration and washed with water and acetone to give cis-dichloro-(3R)-3-aminopyrrolidine platinum (II) (1.28 g) as pale yellow crystal. The physical properties of the cis-dichloro-(3R)-3-aminopyrrolidine platinum (II) thus obtained are identical with those of the cis-dichloro-(3R)-3-aminopyrrolidine platinum (II) as obtained in the above (1-A).

後処理

  1. customThe precipitated solid is removed by filtration
  2. concentrationthe filtrate is concentrated under reduced pressure
  3. additionTo the residue is added water (3 ml)
  4. customthe resulting crystals are separated by filtration
  5. washwashed with water and acetone

出典と根拠

ORDレコード
ord-bfc6683b3622498e8a0c4b120b1c4e54
出典データセット
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04939256

反応ノート

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