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

Water → HCID 67106795、化合物

HRID 1623674
ノート
印刷プレビュー

反応式

HRID 1623674 の反応式
[C:1](Cl)(=O)C(Cl)=O.[CH3:7][O:8][C:9]([C:11]1[CH:12]=[C:13]([CH:17]=[CH:18][C:19]=1[O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:14]([OH:16])=O)=[O:10].CN1[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]1.O>ClCCl.CN(C)C=O>[C:22]1([CH2:21][O:20][C:19]2[CH:18]=[CH:17][C:13]([C:14]([N:32]3[CH2:33][CH2:34][CH2:1][CH2:30][CH2:31]3)=[O:16])=[CH:12][C:11]=2[C:9]([O:8][CH3:7])=[O:10])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1
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 962WaterHCID 531671-MethylpiperazineHCID 65578Oxalyl chlorideHCID 671067771285516-45-1

生成物 1

HCID 67106795HCID 67106795、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide触媒HCID 6344
Dichloromethane
溶媒
2 回

実験手順

Oxalyl chloride (0.61 ml, 6.99 mmol) was added dropwise to a stirred solution of 3-[(methyloxy)carbonyl]-4-[(phenylmethyl)oxy]benzoic acid (may be prepared as described in Description 49; 400 mg, 1.40 mmol) in dichloromethane (10 ml) and dimethylformamide (3 drops) at room temperature. The mixture was stirred at room temperature for 1 h. The solvent was then removed and the residue was dissolved in dichloromethane (5 ml). This mixture was added to a solution of 1-methylpiperazine (525 mg, 5.24 mmol) in dichloromethane (5 ml). The mixture was stirred at room temperature for 2 h. Water (60 ml) was added to the mixture, which was then extracted with dichloromethane (3×60 ml). The organic phase was washed with saturated brine (50 ml), dried over sodium sulfate and evaporated in vacuo to give the crude product. The crude product was loaded onto a silica gel (200 g) column and eluted with dichloromethane/methanol=50:1 to yield the title compound as a colourless oil. 450 mg.

後処理

  1. customThe solvent was then removed
  2. dissolutionthe residue was dissolved in dichloromethane (5 ml)
  3. stirringThe mixture was stirred at room temperature for 2 h
  4. extractionwas then extracted with dichloromethane (3×60 ml)
  5. washThe organic phase was washed with saturated brine (50 ml)
  6. dry with materialdried over sodium sulfate
  7. customevaporated in vacuo
  8. customto give the crude product
  9. washeluted with dichloromethane/methanol=50:1

出典と根拠

ORDレコード
ord-e7f3f9ca94c149c2b8c3c04e87b8cbab
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08778939B2

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