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

Toluene → N5-Allyl-6-chloro-1-methyl-N2-{2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}-1H-indole-2,5-dicarboxamide

HRID 339123
ノート
印刷プレビュー

反応式

HRID 339123 の反応式
[CH2:1]([NH2:4])[CH:2]=[CH2:3].C[Al](C)C.C1(C)C=CC=CC=1.[Cl:16][C:17]1[CH:25]=[C:24]2[C:20]([CH:21]=[C:22]([C:27](=[O:44])[NH:28][CH:29]([C:34]3[CH:39]=[CH:38][CH:37]=[C:36]([C:40]([F:43])([F:42])[F:41])[CH:35]=3)[C:30]([F:33])([F:32])[F:31])[N:23]2[CH3:26])=[CH:19][C:18]=1[C:45](OCC)=[O:46]>ClCCl.O>[CH2:1]([NH:4][C:45]([C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][C:17]=1[Cl:16])[N:23]([CH3:26])[C:22]([C:27]([NH:28][CH:29]([C:34]1[CH:39]=[CH:38][CH:37]=[C:36]([C:40]([F:42])([F:43])[F:41])[CH:35]=1)[C:30]([F:31])([F:32])[F:33])=[O:44])=[CH:21]2)=[O:46])[CH:2]=[CH2:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 1140TolueneHCID 7853AllylamineHCID 16682925TrimethylaluminumHCID 58247953Ethyl 6-chloro-1-methyl-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylate

生成物 1

HCID 58247974N5-Allyl-6-chloro-1-methyl-N2-{2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}-1H-indole-2,5-dicarboxamide

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

Allylamine (156 mg, 2.73 mmol) was dissolved in 3 ml of dichloromethane and admixed dropwise under argon with a solution of trimethylaluminium in toluene (2 M, 1.37 ml, 2.73 mmol). The mixture was stirred for 30 min, and then ethyl 6-chloro-1-methyl-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylate (165 mg, 0.27 mmol) dissolved in 3 ml of dichloromethane was added dropwise. The mixture was heated under reflux overnight and, after cooling to room temperature, water was added cautiously. The mixture was extracted with ethyl acetate, the organic phase washed with potassium sodium tartrate solution, dried over magnesium sulphate and filtered, and the filtrate concentrated under reduced pressure. The purification was effected by means of silica gel chromatography with the eluent cyclohexane/ethyl acetate (EA) (0% EA to 30% EA).

後処理

  1. additionwas added dropwise
  2. temperatureThe mixture was heated
  3. temperatureunder reflux overnight
  4. extractionThe mixture was extracted with ethyl acetate
  5. washthe organic phase washed with potassium sodium tartrate solution
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. concentrationthe filtrate concentrated under reduced pressure
  9. customThe purification

出典と根拠

ORDレコード
ord-65d10d6eb81c43edb7986916d00b99ac
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889878B2

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