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

Ethylenediamine → Agn-PC-0niccc

HRID 1604981
ノート
印刷プレビュー

反応式

HRID 1604981 の反応式
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[C:3]([CH2:10][C:11]#[N:12])=[N:2]1.[CH2:13](N)[CH2:14][NH2:15].C(=S)=S.C(Cl)(Cl)[Cl:21]>>[ClH:21].[NH:12]1[CH2:13][CH2:14][N:15]=[C:11]1[CH2:10][C:3]1[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[O:1][N:2]=1
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 4

HCID 3301EthylenediamineHCID 6212ChloroformHCID 6348Carbon DisulfideHCID 3236401,2-Benzisoxazole-3-acetonitrile

生成物 1

HCID 12279087Agn-PC-0niccc

実験手順

A mixture of 1,2-benzisoxazole-3-acetonitrile (1.6 g), ethylenediamine (0.7 g) and carbon disulfide (0.2 ml) was heated at 130° to 150°C for 0.5 hour and then allowed to stand at room temperature overnight. to the reaction mixture was added chloroform and the insoluble substance was filtered off. The filtrate was subjected to silica gel column chromatography and eluted with 10 to 20 % methanol-chloroform. The eluates were collected and treated with ethanolic hydrochloric acid to give the hydrochloride. The product was treated with charcoal and then recrystallized from ethanol to give the desired compound (0.4 g). m.p. 223° to 228°C.

後処理

  1. temperaturewas heated at 130° to 150°C for 0.5 hour
  2. filtrationthe insoluble substance was filtered off
  3. washeluted with 10 to 20 % methanol-chloroform
  4. customThe eluates were collected
  5. additiontreated with ethanolic hydrochloric acid

出典と根拠

ORDレコード
ord-9d4bb807d28d4ad093f6ee52073c8e34
出典データセット
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03948928

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート