Dicyanamide → 2-Methyl 3-(1-N-pyrrolidinyl-3-cyanopropyl)pyridine

HRID 262957

反応式

HRID 262957 の反応式
C1(S([O-])(=O)=O)C=CC=CC=1.C(C[N+:14]1([CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22]N=2)[CH2:18][CH2:17][CH2:16][CH2:15]1)#N.Br[CH2:27][CH2:28][C:29]#[N:30].[C:31](NC#N)#[N:32].[BH4-].[Na+]>C(O)C>[CH3:22][C:23]1[C:24]([CH2:25][CH2:20][CH:19]([N:14]2[CH2:15][CH2:16][CH2:17][CH2:18]2)[C:31]#[N:32])=[CH:27][CH:28]=[CH:29][N:30]=1

参加物

6

反応物 4

HCID 10443DicyanamideHCID 170203-BromopropionitrileHCID 4311764Sodium borohydrideHCID 5458873(1-(2-Pyridinylmethyl)-15-pyrrolidin-1-yl)acetonitrile benzenesulfonate

生成物 1

HCID 233444222-Methyl 3-(1-N-pyrrolidinyl-3-cyanopropyl)pyridine

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

1-cyanomethyl-1-(2-picolyl)pyrrolidinium benzenesulfonate (see Preparation II) is rearranged and alkylated with 3-bromopropionitrile as in Example 2. The resulting dicyanoamine is decyanated with sodium borohydride in ethanol to give the product. Purification is effected via the picrate.

後処理

  1. customto give the product
  2. customPurification

出典と根拠

ORDレコード
ord-b9926c1df1834cbca7925da2b9609475
出典データセット
uspto-grants-1979_05
特許番号
US04155909

関連ノート

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