Pyridine → N-(2-(piperidin-1-yl)phenyl)isoxazole-5-carboxamide

HRID 33464

反応式

HRID 33464 の反応式
C1C=CC(CNS(C2C=CC3N=NN(O)C=3C=2)(=O)=O)=CC=1.Cl.N1C=CC=CC=1.[O:29]1[C:33]([C:34](Cl)=[O:35])=[CH:32][CH:31]=[N:30]1.[N:37]1([C:43]2[CH:49]=[CH:48][CH:47]=[CH:46][C:44]=2[NH2:45])[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38]1>O1CCCC1.ClCCl>[N:37]1([C:43]2[CH:49]=[CH:48][CH:47]=[CH:46][C:44]=2[NH:45][C:34]([C:33]2[O:29][N:30]=[CH:31][CH:32]=2)=[O:35])[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38]1

参加物

7

実験手順

To PS-HOBt resin (0.1 mmol) was added anhydrous dichloromethane (“DCM”) (1 mL) followed by pyridine (0.5 mmol) and isoxazole-5-carbonyl chloride (Lancaster) (0.3 mmol). The mixture was shaken at room temperature for 3 h and was then filtered. The resin was washed successively with tetrahydrofuran (“THF”) (3×) and DCM (3×) and dried in vacuo. To this acylated resin was added a solution of 2-piperidinoaniline (Lancaster) (0.05 mmol, 0.5 eq) in anhydrous THF (1 mL) and the mixture was shaken at room temperature for 16 h. The mixtue was then filtered and the resin washed with THF and DCM as described above. The combined filtrate and washings were concentrated under reduced pressure to yield the product. Yield: 100%. MS: 272 (M+1). LC/MS purity: 100%. 1HNMR (CDCl3, 300 MHz): δ 8.2 (d, 1H), 7.85 (t, 2H), 7.55 (m, 1H), 7.4 (m, 2H), 3.8-3.2 (bm, 4H), 2.7-1.9 (bm, 4H).

後処理

  1. filtrationwas then filtered
  2. washThe resin was washed successively with tetrahydrofuran (“THF”) (3×) and DCM (3×)
  3. customdried in vacuo
  4. stirringthe mixture was shaken at room temperature for 16 h
  5. filtrationThe mixtue was then filtered
  6. washthe resin washed with THF and DCM
  7. concentrationThe combined filtrate and washings were concentrated under reduced pressure
  8. customto yield the product

出典と根拠

ORDレコード
ord-cc1fc177866d45a0b0846b9269bdeffc
出典データセット
uspto-grants-2008_09
特許番号
US07429603B2

関連ノート

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