Dimethylformamide → HCID 178469972、化合物

HRID 1026904ノート

反応式

HRID 1026904 の反応式
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]2[C:14]([OH:15])=[C:13]([C:16]([OH:18])=[O:17])[CH:12]=[N:11][C:10]=12)=[O:5])[CH3:2].S(Cl)(Cl)=O.[CH3:23]N(C=O)C.C(N(CC)CC)C>ClCCCl.CO>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]2[C:14]([OH:15])=[C:13]([C:16]([O:18][CH3:23])=[O:17])[CH:12]=[N:11][C:10]=12)=[O:5])[CH3:2]

参加物

7

反応物 4

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 24386Thionyl ChlorideHCID 178469973HCID 178469973、化合物

生成物 1

HCID 178469972HCID 178469972、化合物収率 95%

試薬・触媒・溶媒 2

HCID 111,2-Dichloroethane溶媒HCID 887Methanol溶媒

実験手順

3-Ethoxycarbonyl-7-hydroxypyrazolo[1,5-a]pyrimidine-6-carboxylic acid (27.0 g, 0.11 mol) obtained in Example 19, step 2 was suspended in 1,2-dichloroethane (320 mL), and thionyl chloride (39 mL, 0.54 mol) was added. DMF (22 mL) was added, and the mixture was heated under reflux for 6 hr. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was suspended in methylene chloride (300 mL), and triethylamine (75 mL, 0.54 mol) was added in an ice bath. Methanol (50 mL) was added dropwise over 30 min, and the mixture was stirred at room temperature for 2 hr. The solvent was evaporated under reduced pressure, and the residue was added to 2 mol/L hydrochloric acid containing ice (about 500 mL). The precipitated solid was collected by filtration, and washed with water (50 mL) to give the title compound (27.5 g, 95%).

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 6 hr
  3. customthe solvent was evaporated under reduced pressure
  4. customThe solvent was evaporated under reduced pressure
  5. additionthe residue was added to 2 mol/L hydrochloric acid
  6. additioncontaining ice (about 500 mL)
  7. filtrationThe precipitated solid was collected by filtration
  8. washwashed with water (50 mL)

出典と根拠

ORDレコード
ord-e76557fb39c242b0896e3d03319b1be1
出典データセット
uspto-grants-2014_05
特許番号
US08729264B2

反応ノート

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