Water → HCID 68779424、化合物

HRID 2263310ノート

反応式

HRID 2263310 の反応式
[CH3:1][C:2]1[C:6]([CH3:7])=[C:5]([NH:8][C:9](=[O:16])OCC(Cl)(Cl)Cl)[O:4][N:3]=1.[N:17]1([C:23]2[S:24][CH:25]=[C:26]([C:28]3[CH:29]=[C:30]([CH:33]=[CH:34][CH:35]=3)[C:31]#[N:32])[N:27]=2)[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1.C(N(C(C)C)CC)(C)C.O>CS(C)=O>[C:31]([C:30]1[CH:29]=[C:28]([C:26]2[N:27]=[C:23]([N:17]3[CH2:22][CH2:21][N:20]([C:9]([NH:8][C:5]4[O:4][N:3]=[C:2]([CH3:1])[C:6]=4[CH3:7])=[O:16])[CH2:19][CH2:18]3)[S:24][CH:25]=2)[CH:35]=[CH:34][CH:33]=1)#[N:32]

参加物

6

反応物 4

HCID 962WaterHCID 81531DiisopropylethylamineHCID 639931083-(2-Piperazin-1-yl-1,3-thiazol-4-yl)benzonitrileHCID 862452572,2,2-Trichloroethyl(3,4-dimethylisoxazol-5-yl)carbamate

生成物 1

HCID 68779424HCID 68779424、化合物収率 39.6%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
70 °C

実験手順

A mixture of 2,2,2-trichloroethyl (3,4-dimethylisoxazol-5-yl)carbamate (277 mg, 0.964 mmol), 3-(2-piperazin-1-yl-1,3-thiazol-4-yl)benzonitrile (237 mg, 0.877 mmol) and diisopropylethylamine (0.305 ml, 1.75 mmol) in dimethyl sulfoxide (2.9 ml) was stirred at 70° C. for 15 hours. Water was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with water, and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1), and recrystallized from a mixed solvent of hexane and ethyl acetate to give 142 mg (39.6%) of the desired product as a solid.

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with water
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1)
  6. customrecrystallized from a mixed solvent of hexane and ethyl acetate

出典と根拠

ORDレコード
ord-5fdf0702a89144a1ba4542a2a17a5a97
出典データセット
uspto-grants-2010_12
特許番号
US07851473B2

反応ノート

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