Acetone → 7-Methyl-2-(methylthio)pyrido[2,3-d]pyrimidine

HRID 522713

反応式

HRID 522713 の反応式
[NH2:1][C:2]1[C:7]([CH:8]=O)=[CH:6][N:5]=[C:4]([S:10][CH3:11])[N:3]=1.[OH-].[K+].[CH3:14][C:15]([CH3:17])=O>>[CH3:17][C:15]1[CH:14]=[CH:8][C:7]2[CH:6]=[N:5][C:4]([S:10][CH3:11])=[N:3][C:2]=2[N:1]=1

参加物

4

反応物 3

HCID 180AcetoneHCID 14797Potassium HydroxideHCID 2957694-Amino-2-(methylsulfanyl)pyrimidine-5-carbaldehyde

生成物 1

HCID 866970117-Methyl-2-(methylthio)pyrido[2,3-d]pyrimidine

実験手順

Treat a solution of 4-amino-2-(methylthio)pyrimidine-5-carbaldehyde (10 g, 59.1 mmol) in acetone (100 mL) with KOH (3.32 g, 59.1 mmol), stir at RT for 10 min, then concentrate to dryness. Treat the residue with EtOAc, wash with saturated. Aqueous NaHCO3, then brine, dry over Na2SO4 and concentrate to obtain 7-methyl-2-(methylthio)pyrido[2,3-d]pyrimidine. MS (m/z): 192.1 (M+1). Add a solution of methylamine in ethanol (33%, 80 mL) and heat at 110° C. overnight in a pressure tube. Remove the solvent under reduced pressure and purify the crude product by silica gel chromatography (50-100% EtOAc/Hexanes) to obtain the title compound (6.73 g, 65%, over two steps). MS (m/z): 175.1 (M+1).

後処理

  1. concentrationconcentrate to dryness
  2. additionTreat the residue with EtOAc
  3. washwash with saturated
  4. dry with materialAqueous NaHCO3, then brine, dry over Na2SO4
  5. concentrationconcentrate

出典と根拠

ORDレコード
ord-b3a7bc3c52ca414bb9b962cc9b38d56d
出典データセット
uspto-grants-2016_05
特許番号
US09334267B2

関連ノート

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