ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Putrescine → 6-[(4-Aminobutyl)amino]-3-pyridinecarbonitrile

HRID 2281965
ノート
印刷プレビュー

反応式

HRID 2281965 の反応式
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1.[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH2:15]>>[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=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

3

反応物 2

HCID 1045PutrescineHCID 51520946-Chloro-3-pyridinecarbonitrile

生成物 1

HCID 570445896-[(4-Aminobutyl)amino]-3-pyridinecarbonitrile

反応条件

温度
170 °C

実験手順

6-Chloro-3-pyridinecarbonitrile (5.0 g) was dissolved in 1,4-diaminobutane (50 ml), and the solution was stirred at 170° C. for 2 hours with heating. Diethyl ether and distilled water were added to the reaction mixture, the layers were separated, and the aqueous layer was extracted with diethyl ether. The aqueous layer was saturated with sodium chloride, and the resulting mixture was extracted with chloroform. The resulting organic layer was dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain the title compound (4.77 g).

後処理

  1. temperaturewith heating
  • distillationDiethyl ether and distilled water
  • additionwere added to the reaction mixture
  • customthe layers were separated
  • extractionthe aqueous layer was extracted with diethyl ether
  • extractionthe resulting mixture was extracted with chloroform
  • dry with materialThe resulting organic layer was dried over anhydrous magnesium sulfate
  • filtrationfiltered
  • concentrationthe filtrate was concentrated under reduced pressure
  • 出典と根拠

    ORDレコード
    ord-d55adc20c14845db9834123deff5324f
    出典データセット
    uspto-grants-2015_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US09139609B2

    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