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

Selectfluor → HCID 59756548、化合物

HRID 2405753
ノート
印刷プレビュー

反応式

HRID 2405753 の反応式
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([NH2:13])=[C:9]([Cl:12])[CH:10]=2)[CH:5]=[CH:4][N:3]=1.[B-](F)(F)(F)[F:15].[B-](F)(F)(F)F.C1[N+]2(CCl)CC[N+](F)(CC2)C1>CN(C=O)C>[Cl:1][C:2]1[C:11]2[C:6](=[C:7]([F:15])[C:8]([NH2:13])=[C:9]([Cl:12])[CH:10]=2)[CH:5]=[CH:4][N:3]=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 2724933SelectfluorHCID 59756561HCID 59756561、化合物

生成物 1

HCID 59756548HCID 59756548、化合物収率 60%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 2.62 g (12.3 mmol) of 1,7-dichloro-isoquinolin-6-ylamine in DMF (130 mL) was added 5.5 g (15.5 mmol) of Selectfluor® as a solid in one portion. The mixture was stirred at room temperature for 15 h. The mixture was poured over ice and stirred until all of the ice had melted during which time a solid precipitated from solution. The brown solid was collected by filtration, washed with water and dried on the filter pad to provide 1.0 g (60% by 1H-NMR, 21%) of 1,7-dichloro-5-fluoro-isoquinolin-6-ylamine. MS calc. for C9H5Cl2FN2 [M]+: 231.05. Found: 231.68.

後処理

  1. additionThe mixture was poured over ice
  2. customprecipitated from solution
  3. filtrationThe brown solid was collected by filtration
  4. washwashed with water
  5. customdried on the filter pad

出典と根拠

ORDレコード
ord-85fb4fcfdcfc4ec6a7d98ffe89c7c0b0
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08809326B2

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