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Diisopropylethylamine → HCID 178434563、化合物

HRID 522079
ノート
印刷プレビュー

反応式

HRID 522079 の反応式
CN(C(O[N:9]1[N:17]=[N:16][C:11]2[CH:12]=[CH:13]C=N[C:10]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[Cl:25][C:26]1[CH:48]=[CH:47][C:46]([C:49]2[C:54]([F:55])=[CH:53][CH:52]=[CH:51][N:50]=2)=[CH:45][C:27]=1[C:28]([NH:30][C:31]1[N:35]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=2)[N:34]=[C:33]([C:42](O)=[O:43])[CH:32]=1)=[O:29].CCN(C(C)C)C(C)C.CC1C(N)=CNN=1>CN(C=O)C.CCOC(C)=O>[Cl:25][C:26]1[CH:48]=[CH:47][C:46]([C:49]2[C:54]([F:55])=[CH:53][CH:52]=[CH:51][N:50]=2)=[CH:45][C:27]=1[C:28]([NH:30][C:31]1[N:35]([C:36]2[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=2)[N:34]=[C:33]([C:42]([NH:16][C:11]2[C:12]([CH3:13])=[N:17][NH:9][CH:10]=2)=[O:43])[CH:32]=1)=[O:29]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 1184971095-(2-chloro-5-(3-fluoropyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acidHCID 178434557HCID 178434557、化合物

生成物 1

HCID 178434563HCID 178434563、化合物
収率 29.5%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of HATU (0.3 mmol, 113 mg) and 5-(2-chloro-5-(3-fluoropyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acid (Example 105, 0.23 mmol, 100 mg) in DMF (0.9 mL) was added DIPEA (1.10 mmol, 0.191 mL). The solution was stirred at room temperature for 15 minutes. 3-methyl-1H-pyrazol-4-amine (0.23 mmol, 100 mg) was added and the reaction stirred at room temperature for 18 hours. The reaction was diluted with EtOAc (20 mL), washed with NaHCO3 (20 mL), 10% aqueous citric acid solution (20 mL) and brine (20 mL). The organic layer was dried over sodium sulphate and concentrated in vacuo. The residue was purified using reverse phase column chromatography to afford the title compound as a yellow solid (35 mg, 29%).

後処理

  1. stirringthe reaction stirred at room temperature for 18 hours
  2. washwashed with NaHCO3 (20 mL), 10% aqueous citric acid solution (20 mL) and brine (20 mL)
  3. dry with materialThe organic layer was dried over sodium sulphate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified

出典と根拠

ORDレコード
ord-b079327898c0470c86cfb8b5e3eb952a
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09328096B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート