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

N-Methyl-2,2'-diaminodiethylamine → 6-chloropyrazine-2-carboxamide

HRID 1165439
ノート
印刷プレビュー

反応式

HRID 1165439 の反応式
NCCN(C)CCN.N[C:10]1[C:11]([C:18]([N:20]2C=CN=C2)=[O:19])=[N:12][C:13]([Cl:17])=[C:14](N)[N:15]=1>O1CCCC1>[Cl:17][C:13]1[N:12]=[C:11]([C:18]([NH2:20])=[O:19])[CH:10]=[N:15][CH:14]=1
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 430288N-Methyl-2,2'-diaminodiethylamineHCID 13020010(3,5-diamino-6-chloropyrazin-2-yl)(1H-imidazol-1-yl)methanone

生成物 1

HCID 12825296-chloropyrazine-2-carboxamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred solution of 84.0 g (0.744 mol) of N-(2-aminoethyl)-N-methyl-1,2-ethanediamine (see U.S. Pat. No. 3,201,472 for an example of how to obtain this material) in 700 ml of tetrahydrofuran was added 88.6 g (0.372 mol) of 1-(3,5-diamino-6-chloropyrazinoyl)imidazole in 10 portions over 1.5 hours. After 1 hour at ambient temperature the reaction mixture was filtered and concentrated to 300 ml. The solution was added dropwise to 1.4 liters of ether with vigorous stirring. The solid was filtered, washed with ether and dried. There was obtained 74.3 g (0.258 mol, 70%) of 3,5-diamino-N-2-[(2-aminoethyl)methylamino]ethyl]-6-chloropyrazinecarboxamide. A sample was filtered through a pad of silica gel and eluted with 5:95 (v/v) methanol:methylene chloride saturated wth ammonia gas; mp 138°-139.5° C.

後処理

  1. filtrationAfter 1 hour at ambient temperature the reaction mixture was filtered
  2. concentrationconcentrated to 300 ml
  3. additionThe solution was added dropwise to 1.4 liters of ether with vigorous stirring
  4. filtrationThe solid was filtered
  5. washwashed with ether
  6. customdried

出典と根拠

ORDレコード
ord-4087a0faaa5647cf920659a9438cc31b
出典データセット
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04910202

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