4-Toluenesulfonyl chloride → 6,6-Dimethyl-2-nitro-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazine

HRID 1022239ノート

反応式

HRID 1022239 の反応式
O[CH2:2][C:3]1[N:7]([CH2:8][C:9]([CH3:12])([OH:11])[CH3:10])[N:6]=[C:5]([N+:13]([O-:15])=[O:14])[CH:4]=1.[H-].[Na+].C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[Cl-].[NH4+]>CN(C=O)C>[CH3:10][C:9]1([CH3:12])[O:11][CH2:2][C:3]2=[CH:4][C:5]([N+:13]([O-:15])=[O:14])=[N:6][N:7]2[CH2:8]1

参加物

6

反応物 4

HCID 73974-Toluenesulfonyl chlorideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 866840171-(5-(Hydroxymethyl)-3-nitro-1H-pyrazol-1-yl)-2-methylpropan-2-ol

生成物 1

HCID 866840186,6-Dimethyl-2-nitro-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazine収率 22.7%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 330e (1.1 g, 5.1 mmol) in DMF (10 mL), was added NaH (60 percent dispersion in mineral oil, 246 mg, 6.14 mmol) at 0° C. The resulting suspension was stirred for 30 min, followed by the addition of p-toluenesulfonyl chloride (1169 mg, 6.14 mmol). The mixture was stirred at 60° C. overnight. After cooling to room temperature, saturated ammonium chloride solution was added and the mixture was extracted with dichloromethane. The combined organic layer was washed with brine, dried over Na2SO4, and evaporated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with petroleum ether/ethyl acetate gradient (9:1 to 2:1) to afford 330f (228 mg, 22%). MS-ESI: [M+H]+ 198.3

後処理

  1. stirringThe mixture was stirred at 60° C. overnight
  2. extractionthe mixture was extracted with dichloromethane
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. customevaporated under reduced pressure
  6. customThe residue was purified by silica-gel column chromatography
  7. washeluting with petroleum ether/ethyl acetate gradient (9:1 to 2:1)

出典と根拠

ORDレコード
ord-ef9c36aef1bb40ca8be375b3f3e5ed30
出典データセット
uspto-grants-2014_05
特許番号
US08716274B2

反応ノート

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