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-Iodosuccinimide → 3-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridine

HRID 588412
ノート
印刷プレビュー

反応式

HRID 588412 の反応式
[CH3:1][C:2]1[NH:10][C:5]2=[CH:6][N:7]=[CH:8][CH:9]=[C:4]2[CH:3]=1.[I:11]N1C(=O)CCC1=O>C(Cl)(Cl)Cl>[I:11][C:3]1[C:4]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[NH:10][C:2]=1[CH3:1]
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 120273N-IodosuccinimideHCID 124075052-Methyl-1H-pyrrolo(2,3-c)pyridine

生成物 1

HCID 674185123-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridine収率 92%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

2-Methyl-1H-pyrrolo[2,3-c]pyridine (100 mg, 0.76 mmol) was dissolved in CHCl3 (5 mL), N-iodosuccinimide (179 mg, 0.79 mmol) was added and the reaction mixture was stirred for 2 h. The reaction mixture was quenched with 1 M aq sodium thiosulphate (5 mL) and the CHCl3 was removed in vacuo. The reaction mixture was partitioned between sat aq NaHCO3 (40 mL) and EtOAc (40 mL). The aqueous layer was extracted with EtOAc (40 mL) and the combined organic fractions were washed with sat aq NaHCO3 (50 mL) and brine (50 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a cream solid (179 mg, 92%). LCMS (ES+): 258.9 (M+H)+.

後処理

  1. customThe reaction mixture was quenched with 1 M aq sodium thiosulphate (5 mL)
  2. customthe CHCl3 was removed in vacuo
  3. customThe reaction mixture was partitioned
  4. extractionThe aqueous layer was extracted with EtOAc (40 mL)
  5. washthe combined organic fractions were washed with sat aq NaHCO3 (50 mL) and brine (50 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-0bc03b6cdbca44099e42bb0342e9bb07
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09227967B2

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