Dimethylformamide → 1h-Pyrazolo[4,3-b]pyridine-5,6-dicarboxylic acid,1-methyl-,5,6-dimethyl ester

HRID 1734436

反応式

HRID 1734436 の反応式
CN(C)[CH:3]=[O:4].P(Cl)(Cl)(Cl)=[O:7].[CH3:11][N:12]1[CH:16]=[C:15]([NH:17][C:18]([CH2:28]C)=[C:19]([C:24](OC)=O)[C:20]([O:22][CH3:23])=[O:21])[CH:14]=[N:13]1.C[N+](C)=CCl.[Cl-]>ClC(Cl)C>[CH3:11][N:12]1[C:16]2[C:15](=[N:17][C:18]([C:28]([O:4][CH3:3])=[O:7])=[C:19]([C:20]([O:22][CH3:23])=[O:21])[CH:24]=2)[CH:14]=[N:13]1

参加物

6

反応条件

温度
-5 °C

実験手順

Dimethylformamide (7.4 mL, 0.096 mol) is dissolved in 125 mL dichloroethane and the mixture cooled to -5° C. in an acetone/ice bath. Phosphorous oxychloride (8.9 mL, 0.095 mol) is added in one portion and the clear colorless solution is allowed to warm slowly to room temperature, gradually turning yellow. The unpurified dimethyl [(1-methylpyrazol-4-yl)amino]-butenedicarboxylate is dissolved in 75 mL of dichloroethane and added to the chilled Vilsmeier reagent dropwise keeping the reaction temperature below 5° C. The mixture is allowed to warm slowly to room temperature over four hours, and then is heated to reflux for one hour. The mixture is concentrated to a solid which is chromatographed using 3:1 hexanes/ethyl acetate. The fractions containing the desired product are combined and concentrated to give the product as a white solid (16.93 g, 71.4%), melting point 148°-149° C.

後処理

  1. temperatureto warm slowly to room temperature
  2. customthe reaction temperature below 5° C
  3. temperatureto warm slowly to room temperature over four hours
  4. temperatureis heated
  5. temperatureto reflux for one hour
  6. concentrationThe mixture is concentrated to a solid which
  7. customis chromatographed
  8. additionThe fractions containing the desired product
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-e69b768a4d6d46a9b0e5c1854f371580
出典データセット
uspto-grants-1996_07
特許番号
US05534484

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