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

Ammonium Hydroxide → 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxamide

HRID 1696205
ノート
印刷プレビュー

反応式

HRID 1696205 の反応式
[Cl:1][C:2]1[C:7]([C:8](O)=[O:9])=[CH:6][N:5]=[C:4]2[NH:11][CH:12]=[CH:13][C:3]=12.O[N:15]1C2C=CC=CC=2N=N1.CN(C)CCCN=C=NCC.[OH-].[NH4+]>CN(C)C=O.C(Cl)(Cl)Cl.O>[Cl:1][C:2]1[C:7]([C:8]([NH2:15])=[O:9])=[CH:6][N:5]=[C:4]2[NH:11][CH:12]=[CH:13][C:3]=12
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

8

反応物 4

HCID 14923Ammonium HydroxideHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 260764404-Chloro-1H-pyrrolo(2,3-b)pyridine-5-carboxylic acid

生成物 1

HCID 669241774-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxamide収率 10.8%

試薬・触媒・溶媒 3

HCID 962
Water
溶媒
HCID 6212Chloroform溶媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

To a solution of 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylicacid (840 mg) in N,N-dimethylformamide (8.4 mL) were added 1-hydroxybenzotriazole (808 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (929 mg). The mixture was stirred at 60° C. for 30 minutes. The solution was cooled to ambient temperature and added 28% ammonium hydroxide aqueous solution (1.2 mL). The mixture was stirred at ambient temperature for 1 hour. To the solution were added water and chloroform and the mixture was extracted with chloroform. The extract was dried over MgSO4, filtrated and evaporated. The residue was purified by column chromatography on silica gel with chloroform and methanol (100:0 to 90:10) to give 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxamide (90 mg) as a pale yellow powder.

後処理

  1. temperatureThe solution was cooled to ambient temperature
  2. stirringThe mixture was stirred at ambient temperature for 1 hour
  3. extractionthe mixture was extracted with chloroform
  4. dry with materialThe extract was dried over MgSO4
  5. filtrationfiltrated
  6. customevaporated
  7. customThe residue was purified by column chromatography on silica gel with chloroform and methanol (100:0 to 90:10)

出典と根拠

ORDレコード
ord-aee9318ac9c644b2b71c36bd52d719fb
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163767B2

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