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

Tetrahydrofuran → 2-((2S,3R)-3-(3-chlorophenyl)-2-(4-chlorophenyl)-6-oxopiperidin-1-yl)pentanedial

HRID 1048326
ノート
印刷プレビュー

反応式

HRID 1048326 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:8]2[C@@H:13]([C:14]3[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=3)[N:12](C3CCC=C3)[C:11](=[O:26])[CH2:10][CH2:9]2)[CH:5]=[CH:6][CH:7]=1.C[N+]1([O-])CC[O:31][CH2:30]C1.I([O-])(=O)(=O)=O.[Na+].[CH2:41]1[CH2:45][O:44][CH2:43][CH2:42]1>[Os](=O)(=O)(=O)=O.O.CC(O)(C)C>[Cl:1][C:2]1[CH:3]=[C:4]([C@H:8]2[CH2:9][CH2:10][C:11](=[O:26])[N:12]([CH:42]([CH2:41][CH2:45][CH:30]=[O:31])[CH:43]=[O:44])[C@@H:13]2[C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)[CH:5]=[CH:6][CH:7]=1
参加物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 8028TetrahydrofuranHCID 82029Methyl morpholine oxideHCID 23667635Sodium periodateHCID 58573261(5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-(cyclopent-2-enyl)piperidin-2-one

生成物 1

HCID 585737832-((2S,3R)-3-(3-chlorophenyl)-2-(4-chlorophenyl)-6-oxopiperidin-1-yl)pentanedial

試薬・触媒・溶媒 3

HCID 30318
Osmium Tetroxide
触媒
HCID 962Water溶媒2 回
HCID 6386tert-Butanol溶媒

実験手順

To a solution of 454 mg (1.175 mmol) of (5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-(cyclopent-2-enyl)piperidin-2-one (Example 104, Step A) in THF (6 mL) was added water dropwise (3.5 mL) and tBuOH (0.2 mL). 4-methylmorpholine 4-oxide (207 mg, 1.763 mmol) was added followed by 4% aq. osmium(VIII) oxide (37.3 μL, 5.88 μmol). The reaction mixture was stirred at room temperature for 18 h. Sodium periodate (704 mg, 3.29 mmol) was added and the cloudy reaction mixture was stirred at room temperature for 90 min. Water (4 mL) was added and the mixture was filtered and washed with EtOAc. The filtrate was diluted with EtOAc and the layers were separated. The combined organic layers were washed with sat. Na2S2O3, sat. aq. NaCl solution, dried over Na2SO4 and concentrated in vacuo to provide the title compound.

後処理

  1. customthe cloudy reaction mixture
  2. stirringwas stirred at room temperature for 90 min
  3. filtrationthe mixture was filtered
  4. washwashed with EtOAc
  5. additionThe filtrate was diluted with EtOAc
  6. customthe layers were separated
  7. washThe combined organic layers were washed with sat. Na2S2O3, sat. aq. NaCl solution
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-926c9067c3ab41349da26e1b72cfd7e4
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569341B2

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