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6-amino-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-one → HCID 59377423、化合物

HRID 386662
ノート
印刷プレビュー

反応式

HRID 386662 の反応式
[Br-:1].C([N+](C(C)(C)C)(C(C)(C)C)C(C)(C)C)(C)(C)C.[NH2:19][C:20]1[CH:21]=[CH:22][C:23]2[O:28][CH2:27][C:26](=[O:29])[N:25]([CH3:30])[C:24]=2[CH:31]=1>C(Cl)Cl.CO>[NH2:19][C:20]1[C:21]([Br:1])=[CH:22][C:23]2[O:28][CH2:27][C:26](=[O:29])[N:25]([CH3:30])[C:24]=2[CH:31]=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 2

HCID 27644636-amino-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 98185972-Propanaminium, N,N,N-tris(1,1-dimethylethyl)-2-methyl-, bromide

生成物 1

HCID 59377423HCID 59377423、化合物収率 36%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 6344Dichloromethane溶媒

実験手順

Tetra-tert-butyl ammonium bromide (6.77 g, 14.04 mmol) was added to a solution of 6-amino-4-methyl-4H-benzo[1,4]oxazin-3-one (2.5 g, 14.04 mmol) in methylene chloride (100 ml) and MeOH (50 ml). The mixture was stirred at room temperature for 20 minutes, then quenched with aqueous sodium bisulfite solution. The mixture was extracted with methylene chloride, and the combined organic extracts were dried over MgSO4, filtered, concentrated under reduced pressure and purified via column chromatography to give 1.30 g of 6-amino-7-bromo-4-methyl-4H-benzo[1,4]oxazin-3-one as a light yellow solid, 40%.

後処理

  1. customquenched with aqueous sodium bisulfite solution
  2. extractionThe mixture was extracted with methylene chloride
  3. dry with materialthe combined organic extracts were dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. custompurified via column chromatography

出典と根拠

ORDレコード
ord-542b3f87ce0840ea9a032193ac67d623
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08372865B2

反応ノート

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