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Tetrahydrofuran → HCID 178463061、化合物

HRID 640839
ノート
印刷プレビュー

反応式

HRID 640839 の反応式
O[CH:2]=[C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([NH:19][C:20]([C:22]4[N:23]([CH2:28][CH3:29])[N:24]=[C:25]([CH3:27])[CH:26]=4)=[O:21])=[CH:15][CH:14]=3)[CH:10]=2)[NH:5][C:4]1=[O:30].C1COCC1.[CH3:36][N:37]1[CH2:42][CH2:41][N:40]([C:43]2[CH:48]=[CH:47][C:46]([NH2:49])=[CH:45][CH:44]=2)[CH2:39][CH2:38]1>CCOC(C)=O>[CH3:36][N:37]1[CH2:38][CH2:39][N:40]([C:43]2[CH:48]=[CH:47][C:46]([NH:49][CH:2]=[C:3]3[C:11]4[C:6](=[CH:7][CH:8]=[C:9]([CH2:12][C:13]5[CH:14]=[CH:15][C:16]([NH:19][C:20]([C:22]6[N:23]([CH2:28][CH3:29])[N:24]=[C:25]([CH3:27])[CH:26]=6)=[O:21])=[CH:17][CH:18]=5)[CH:10]=4)[NH:5][C:4]3=[O:30])=[CH:45][CH:44]=2)[CH2:41][CH2:42]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 7372534-(4-Methylpiperazin-1-yl)anilineHCID 1784630622-ethyl-N-[4-[[3-(hydroxymethylidene)-2-oxo-1H-indol-5-yl]methyl]phenyl]-5-methylpyrazole-3-carboxamide

生成物 1

HCID 178463061HCID 178463061、化合物収率 55%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
65 °C

実験手順

A small screw cap test tube was charged with 2-Ethyl-5-methyl-2H-pyrazole-3-carboxylic acid [4-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indol-5-ylmethyl)-phenyl]-amide (prepared below, 70 mg, 0.175 mmol) and THF (1 mL). To the resulting solution was added 4-(4-Methyl-piperazin-1-yl)-phenylamine (66.8 mg, 0.349 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and then diluted with EtOAc (2 mL). The solution was washed with water (2 mL) and the water layer was re-washed with additional EtOAc (2 mL). The combined organic layers were then concentrated in vacuo affording the crude product. The crude product was further purified by silica gel column chromatography with 5% methanol in chloroform as eluant to give the desired product as a solid in 55% yield (55 mg, 0.96 mmol).

後処理

  1. customA small screw cap test tube
  2. temperatureSubsequently, the reaction mixture was cooled to room temperature
  3. washThe solution was washed with water (2 mL)
  4. washthe water layer was re-washed with additional EtOAc (2 mL)
  5. concentrationThe combined organic layers were then concentrated in vacuo
  6. customaffording the crude product
  7. customThe crude product was further purified by silica gel column chromatography with 5% methanol in chloroform as eluant

出典と根拠

ORDレコード
ord-099d4d3b51ce4054b735b54975d1806d
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07692005B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート