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

3-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione → 3-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione

HRID 1031574
ノート
印刷プレビュー

反応式

HRID 1031574 の反応式
Cl.N1C=CC=CC=1.[CH2:8]([N:15]1[C:21](=[O:22])[CH:20]2[N:23](C)[CH:17]([CH2:18][CH2:19]2)[C:16]1=[O:25])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>O>[CH2:8]([N:15]1[C:16](=[O:25])[CH:17]2[NH:23][CH:20]([CH2:19][CH2:18]2)[C:21]1=[O:22])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=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 2868213-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane-2,4-dioneHCID 10176127Pyridinium chloride

生成物 1

HCID 148395753-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione収率 50%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In a dry flask were mixed 15 g of dry pyridine hydrochloride and 3.15 g (130 mmol) of 3-benzyl-2,4-dioxo-8-methyl-3,8-diazabicyclo [3.2.1] octane prepared according to U.S. Pat. No. 3,328,398 in 1967, Jun. 27. The mixture was heated in an oil bath preheated at 220° C. for 20 mn, cooled in an ice-bath, dissolved in 90 ml water, extracted four times with 100 ml ethyl ether. The organic layers were collected and dried over magnesium sulfate. After removing the solvent, the residue was chromatographied over silica-gel using dichloromethane/ethylacetate (80:20) to afford 1.5 g of the title compound (50%). M.P. 72° C.

後処理

  1. customprepared
  2. temperatureThe mixture was heated in an oil bath
  3. custompreheated at 220° C. for 20 mn
  4. temperaturecooled in an ice-bath
  5. extractionextracted four times with 100 ml ethyl ether
  6. customThe organic layers were collected
  7. dry with materialdried over magnesium sulfate
  8. customAfter removing the solvent

出典と根拠

ORDレコード
ord-51b4efaf71b94ff69d31680fde10eaa3
出典データセット
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04954507

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