Nitrourea → Dezinamide

HRID 974582

反応式

HRID 974582 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[O:6][CH:7]1[CH2:10][NH:9][CH2:8]1.[N+]([NH:19][C:20](N)=[O:21])([O-])=O>CC(C)=O>[F:15][C:2]([F:1])([F:14])[C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[O:6][CH:7]1[CH2:10][N:9]([C:20]([NH2:19])=[O:21])[CH2:8]1

参加物

4

反応物 2

HCID 62372NitroureaHCID 111385383-[3-(Trifluoromethyl)phenoxy]azetidine

生成物 1

HCID 146291Dezinamide

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A mixture of 30.6 g (0.141 mole) of 3-[3-(trifluoromethyl)phenoxy]azetidine and 42 g (0.321 mole) of nitrourea (80%) in 500 ml of acetone was stirred for 5 days (5 days not required, but convenient) at room temperature. The mixture was filtered and the filtrate concentrated in vacuo. The residue was partitioned between 150 ml of water and 100 ml of ethyl acetate and the layers separated. The aqueous layer was washed with 100 ml of ethyl acetate. The ethyl acetate layers were washed with 75 ml of 5% aqueous sodium hydroxide solution followed by 75 ml of water, dried over sodium sulfate and concentrated in vacuo. The residual oil was crystallized from ethyl alcohol-ethyl acetate to give 22 g (60%) substantially the title compound. Recrystallization twice from ethyl alcohol gave 9.9 g of white crystalline solid, m.p. 151°-152.5° C.

後処理

  1. customat room temperature
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate concentrated in vacuo
  4. customThe residue was partitioned between 150 ml of water and 100 ml of ethyl acetate
  5. customthe layers separated
  6. washThe aqueous layer was washed with 100 ml of ethyl acetate
  7. washThe ethyl acetate layers were washed with 75 ml of 5% aqueous sodium hydroxide solution
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated in vacuo
  10. customThe residual oil was crystallized from ethyl alcohol-ethyl acetate

出典と根拠

ORDレコード
ord-c8deab93588b4d5995f0d79cf96e7c3e
出典データセット
uspto-grants-1991_11
特許番号
US05068231

関連ノート

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