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Ammonia → 6,7-Dichloro-2,3-dimethoxy-5-(1-methyl-1H-tetrazol-5-yl)quinoxaline

HRID 842668
ノート
印刷プレビュー

反応式

HRID 842668 の反応式
P(Cl)(Cl)(Cl)(Cl)Cl.[Cl:7][C:8]1[C:9]([C:23](=O)[NH:24][CH3:25])=[C:10]2[C:15](=[CH:16][C:17]=1[Cl:18])[N:14]=[C:13]([O:19][CH3:20])[C:12]([O:21][CH3:22])=[N:11]2.C[Si]([N:31]=[N+:32]=[N-:33])(C)C.N>C1(C)C=CC=CC=1>[Cl:7][C:8]1[C:9]([C:23]2[N:24]([CH3:25])[N:33]=[N:32][N:31]=2)=[C:10]2[C:15](=[CH:16][C:17]=1[Cl:18])[N:14]=[C:13]([O:19][CH3:20])[C:12]([O:21][CH3:22])=[N:11]2
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 222AmmoniaHCID 24819Phosphorus pentachlorideHCID 78378AzidotrimethylsilaneHCID 226148716,7-Dichloro-2,3-dimethoxy-5-(N-methylcarbamoyl)quinoxaline

生成物 1

HCID 226148996,7-Dichloro-2,3-dimethoxy-5-(1-methyl-1H-tetrazol-5-yl)quinoxaline収率 38%

試薬・触媒・溶媒 1

HCID 1140
Toluene
溶媒

実験手順

Phosphorous pentachloride (0.136 g, 0.65 mmol) was added to a solution of 6,7-dichloro-2,3-dimethoxy-5-(N-methylcarbamoyl)quinoxaline (Preparation 7, 0.197 g, 0.62 mmol) in toluene (7 mL) and the mixture was heated under reflux under nitrogen for 1 hour. The reaction was cooled to room temperature and trimethylsilyl azide (123 μL, 0.107 g, 0.93 mmol) was added. After stirring at room temperature for 18 hours, dilute aqueous ammonia solution (20 mL) was added and the mixture was extracted with dichloromethane (3×50 mL). The combined organic extracts were dried (MgSO4) and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with dichloromethane to give the title compound (0.080 g, 38%) as a white solid.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux under nitrogen for 1 hour
  3. extractionthe mixture was extracted with dichloromethane (3×50 mL)
  4. dry with materialThe combined organic extracts were dried (MgSO4)
  5. customevaporated under reduced pressure
  6. customThe residue was purified by flash chromatography on silica gel
  7. washeluting with dichloromethane

出典と根拠

ORDレコード
ord-7671fda7fd4049289780734104922aef
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06376490B1

反応ノート

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