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

Triethylamine → HCID 11449562、化合物

HRID 2271354
ノート
印刷プレビュー

反応式

HRID 2271354 の反応式
[CH3:1][N:2]([CH3:19])[C:3]([CH2:5][CH2:6][CH2:7][C:8]#[C:9][C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=1)[C:13]([OH:15])=O)=[O:4].CCN=C=NCCCN(C)C.C(N(CC)CC)C.[F:38][CH2:39][CH2:40][NH2:41]>ClCCl>[CH3:19][N:2]([CH3:1])[C:3]([CH2:5][CH2:6][CH2:7][C:8]#[C:9][C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=1)[C:13]([NH:41][CH2:40][CH2:39][F:38])=[O:15])=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 99962-FluoroethylamineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 114823353-(5-Dimethylcarbamoyl-pent-1-ynyl)-benzoic acid

生成物 1

HCID 11449562HCID 11449562、化合物収率 91%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

To a solution of 3-(5-dimethylcarbamoyl-pent-1-ynyl)-benzoic acid (0.100 g, 0.38 mmol) in dry dichloromethane (1.5 mL) under a nitrogen atmosphere at room temperature, EDCI (0.0728 g, 0.38 mmol) was added followed by triethylamine (0.162 mL, 1.14 mmol), the resulting mixture was stirred at room temperature for further minutes. 2-Fluoro ethylamine (0.189 g, 1.9 mmol) was then added and the mixture stirred at room temperature for 16 hrs. The reaction mixture was washed with a mixture of saturated brine and saturated sodium bicarbonate (1:1; 2×150 mL) followed by saturated brine solution (100 mL). The organic layer was separated and dried over magnesium sulfate and the solvent evaporated under vacuum. The residue was purified by flash column chromatography on silica gel (DCM:MeOH, 95% to 5% methanol gradient) to afford 3-(5-dimethylcarbamoyl-pent-1-ynyl)-N-(2-fluoro-ethyl)benzamide (26) (0.103 g, 0.34 mmol, 91% yield).

後処理

  1. stirringthe mixture stirred at room temperature for 16 hrs
  2. washThe reaction mixture was washed with a mixture of saturated brine and saturated sodium bicarbonate (1:1; 2×150 mL)
  3. customThe organic layer was separated
  4. dry with materialdried over magnesium sulfate
  5. customthe solvent evaporated under vacuum
  6. customThe residue was purified by flash column chromatography on silica gel (DCM:MeOH, 95% to 5% methanol gradient)

出典と根拠

ORDレコード
ord-9eec53e51d1d4e98bb1874aeae6e33ab
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09120723B2

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