Pyridine → 5-(2-m-Tolylsulfanylmethybenzoylamino)-1H-pyrazole-3-carboxylic acid methyl ester

HRID 2114279ノート

反応式

HRID 2114279 の反応式
[NH2:1][C:2]1[N:6](C(OC(C)(C)C)=O)[N:5]=[C:4]([C:14]([O:16][CH3:17])=[O:15])[CH:3]=1.N1C=CC=CC=1.[C:24]1([CH3:41])[CH:29]=[CH:28][CH:27]=[C:26]([S:30][CH2:31][C:32]2[CH:40]=[CH:39][CH:38]=[CH:37][C:33]=2[C:34](Cl)=[O:35])[CH:25]=1>CN(C1C=CN=CC=1)C.C(Cl)Cl>[CH3:17][O:16][C:14]([C:4]1[CH:3]=[C:2]([NH:1][C:34](=[O:35])[C:33]2[CH:37]=[CH:38][CH:39]=[CH:40][C:32]=2[CH2:31][S:30][C:26]2[CH:25]=[C:24]([CH3:41])[CH:29]=[CH:28][CH:27]=2)[NH:6][N:5]=1)=[O:15]

参加物

6

実験手順

A solution of 1.1 eq. of 20, 1.1 eq. of pyridine, and 0.07 eq. of DMAP in CH2Cl2 was cooled to 0° C. While stirring, a solution of 1.0 eq. of 59 in CH2Cl2 was added. The reaction solution was allowed to warm to rt. After a time sufficient for reaction completion, the reaction solution was concentrated by rotary evaporation and 1.0 M HCl was added. The acidified solution was extracted with EtOAc. The combined organic extracts were washed with saturated aqueous NaHCO3, followed by drying over MgSO4 and filtering. The filtrate was rotary evaporated and the crude material was purified by flash chromatography on silica gel using a mixture of EtOAc-hexanes as eluant to give 60.

後処理

  1. customAfter a time sufficient for reaction completion
  2. concentrationthe reaction solution was concentrated by rotary evaporation and 1.0 M HCl
  3. additionwas added
  4. extractionThe acidified solution was extracted with EtOAc
  5. washThe combined organic extracts were washed with saturated aqueous NaHCO3
  6. dry with materialby drying over MgSO4
  7. filtrationfiltering
  8. customThe filtrate was rotary evaporated
  9. customthe crude material was purified by flash chromatography on silica gel using
  10. additiona mixture of EtOAc-hexanes as eluant

出典と根拠

ORDレコード
ord-59f4fa2770974cf5bfbea04cea731130
出典データセット
uspto-grants-2008_10
特許番号
US07432379B2

反応ノート

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