4-(Methylamino)benzoic acid → UP9V9DB2RD

HRID 967775

反応式

HRID 967775 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]2[CH2:18][CH2:17][C:14]3([CH2:16][O:15]3)[CH2:13][CH2:12]2)=[CH:5][CH:4]=1)#[N:2].[CH3:19][NH:20][C:21]1[CH:29]=[CH:28][C:24]([C:25]([OH:27])=[O:26])=[CH:23][CH:22]=1.C(=O)([O-])O.[Na+]>FC(F)(F)S([O-])(=O)=O.[Sc+3].FC(F)(F)S([O-])(=O)=O.FC(F)(F)S([O-])(=O)=O.C(#N)C.O>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]2[CH2:18][CH2:17][C:14]([CH2:16][N:20]([CH3:19])[C:21]3[CH:22]=[CH:23][C:24]([C:25]([OH:27])=[O:26])=[CH:28][CH:29]=3)([OH:15])[CH2:13][CH2:12]2)=[CH:5][CH:4]=1)#[N:2]

参加物

7

反応物 3

HCID 663454-(Methylamino)benzoic acidHCID 516892Sodium BicarbonateHCID 858197211-[2-(4-Cyanophenyl)ethyl]piperidin-4-spiro-2'-oxirane

生成物 1

HCID 12986481UP9V9DB2RD収率 64.5%

試薬・触媒・溶媒 3

HCID 2734571Scandium(III) triflate触媒HCID 962Water溶媒HCID 6342Acetonitrile溶媒2 回

実験手順

Scandium trifluoromethanesulfonate (609 mg) was added to a mixture of the compound (500 mg) obtained in Step 3 of Example 1, 4-methylaminobenzoic acid (343 mg) and anhydrous acetonitrile (10 mL) under cooling with ice-water, and the mixture was stirred at room temperature for sixty eight hours under nitrogen atmosphere. Water (50 mL) and acetonitrile (10 mL) were added to the resulting mixture and the pH of the mixture was adjusted to above 9 with sodium hydrogen carbonate, insoluble matter was removed by filtration and the filtrate was concentrated under reduced pressure. Water in the residue was removed by azeotrope with ethanol, soluble components in the residue were dissolved in ethanol and the insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure and then, the residue was dissolved in water (50 mL) and the pH of the solution was adjusted to 7 by diluted hydrochloric acid. Precipitate was collected by filtration and washed with water and ethyl acetate successively under stirring. The precipitate was collected by filtration and dried to obtain the titled compound (524 mg) as powder.

後処理

  1. customwas removed by filtration
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customWater in the residue was removed by azeotrope with ethanol, soluble components in the residue
  4. dissolutionwere dissolved in ethanol
  5. customthe insoluble matter was removed by filtration
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. dissolutionthe residue was dissolved in water (50 mL)
  8. filtrationPrecipitate was collected by filtration
  9. washwashed with water and ethyl acetate successively
  10. stirringunder stirring
  11. filtrationThe precipitate was collected by filtration
  12. customdried

出典と根拠

ORDレコード
ord-4299d678945a4105be6f8c2c05d2b8d2
出典データセット
uspto-grants-2005_10
特許番号
US06956046B2

関連ノート

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