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

Dimethyl Sulfide → 3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde

HRID 885679
ノート
印刷プレビュー

反応式

HRID 885679 の反応式
[CH:1]([C:9]1[CH:10]=[CH:11][C:12]2[O:13][CH2:14][C:15](=[O:19])[NH:16][C:17]=2[N:18]=1)=CC1C=CC=CC=1.[O:20]=[O+][O-].S(C)C>C(Cl)Cl>[O:19]=[C:15]1[CH2:14][O:13][C:12]2[CH:11]=[CH:10][C:9]([CH:1]=[O:20])=[N:18][C:17]=2[NH:16]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1068Dimethyl SulfideHCID 24823OzoneHCID 684438466-Styryl-4H-pyrido[3,2-b][1,4]oxazin-3-one

生成物 1

HCID 218737373-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 6-styryl-4H-pyrido[3,2-b][1,4]oxazin-3-one (757 mg, 3.00 mmol) in CH2Cl2 (128 mL) was bubbled ozone at −78° C. with stirring until a pale blue color appeared. The excess ozone was removed by bubbling oxygen through the reaction mixture for 15 min. Me2S (1.0 mL, 14 mmol) was added, and the reaction was stirred at −78° C. for 3 h and then at RT for 24 h. The solvent was concentrated and the residue was triturated with Et2O (100 mL). The solid collected from filtration of the suspension was washed with additional Et2O and dried in vacuo to provide 340 mg (63% crude) of a solid, which was used without further purification. MS (ESI): exact mass calculated for C8H6N2O3, 178.04; m/z found, 179.2 [M+H]+.

後処理

  1. customThe excess ozone was removed
  2. customby bubbling oxygen through the reaction mixture for 15 min
  3. stirringthe reaction was stirred at −78° C. for 3 h
  4. concentrationThe solvent was concentrated
  5. customthe residue was triturated with Et2O (100 mL)
  6. filtrationThe solid collected from filtration of the suspension
  7. washwas washed with additional Et2O
  8. customdried in vacuo
  9. customto provide 340 mg (63% crude) of a solid, which
  10. customwas used without further purification

出典と根拠

ORDレコード
ord-208845058ec44ce1b540c6cfc11a8d89
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08242275B2

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