Acetone Cyanohydrin → HCID 178495760、化合物

HRID 1846401ノート

反応式

HRID 1846401 の反応式
[F:1][C:2]1[CH:3]=[C:4]([C:9]2[N:10]([CH2:19][CH2:20][O:21][CH3:22])[C:11](=[O:18])[C:12]([C:15]([OH:17])=O)=[CH:13][N:14]=2)[CH:5]=[C:6]([F:8])[CH:7]=1.C(Cl)(=O)C(Cl)=O.[CH:29]12[CH2:36][CH:33]([CH2:34][CH2:35]1)[C:32](=[O:37])[CH2:31][C:30]2=[O:38].C(N(CC)CC)C.OC(C)(C)C#N>ClCCl.CN(C)C=O>[F:8][C:6]1[CH:5]=[C:4]([C:9]2[N:10]([CH2:19][CH2:20][O:21][CH3:22])[C:11](=[O:18])[C:12]([C:15]([C:31]3[C:32](=[O:37])[CH:33]4[CH2:36][CH:29]([CH2:35][CH2:34]4)[C:30]=3[OH:38])=[O:17])=[CH:13][N:14]=2)[CH:3]=[C:2]([F:1])[CH:7]=1

参加物

8

反応物 5

HCID 6406Acetone CyanohydrinHCID 8471Triethylamine2 回HCID 65578Oxalyl chlorideHCID 144686Bicyclo(3.2.1)octane-2,4-dioneHCID 679550472-(3,5-Difluorophenyl)-1,6-dihydro-1-(2-methoxyethyl)-6-oxo-5-pyrimidinecarboxylic acid2 回

生成物 1

HCID 178495760HCID 178495760、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide触媒HCID 6344Dichloromethane溶媒

実験手順

To 2-(3,5-difluorophenyl)-1,6-dihydro-1-(2-methoxyethyl)-6-oxo-5-pyrimidinecarboxylic acid (i.e. the product from Example 9, Step D) (0.25 g, 0.81 mmol) in 10 mL of dichloromethane was added oxalyl chloride (0.21 g, 1.6 mmol) and one drop of N,N-dimethylformamide. The reaction mixture was stirred at room temperature for 2 h and then concentrated under reduced pressure. The remaining crude oil was re-dissolved in dichloromethane (10 mL) and then treated with bicyclo[3.2.1]octane-2,4-dione (0.12 g, 0.88 mmol) (prepared according to U.S. Pat. No. 6,815,563) and triethylamine (0.16 g, 1.6 mmol). After 30 min at room temperature, a catalytic amount of 2-hydroxy-2-methyl-propanenitrile (0.0075 g, 0.088 mmol) and triethylamine (0.16 g, 1.6 mmol) were added and the reaction mixture was stirred at ambient temperature over night. The reaction mixture was then concentrated under reduced pressure and purified by medium pressure liquid chromatography on silica gel eluting with 0 to 10% methanol in chloroform to provide 0.180 g of the title compound (also known as 3-[[2-(3,5-difluorophenyl)-1,6-dihydro-1-(2-methoxyethyl)-6-oxo-5-pyrimidinyl]carbonyl]biciclo[3.2.1]octane-2,4-dione), a compound of the present invention, as a solid.

後処理

  1. concentrationconcentrated under reduced pressure
  2. dissolutionThe remaining crude oil was re-dissolved in dichloromethane (10 mL)
  3. customprepared
  4. waitAfter 30 min at room temperature
  5. stirringthe reaction mixture was stirred at ambient temperature over night
  6. concentrationThe reaction mixture was then concentrated under reduced pressure
  7. custompurified by medium pressure liquid chromatography on silica gel eluting with 0 to 10% methanol in chloroform

出典と根拠

ORDレコード
ord-7598e3647df4430494a42bdd2e509856
出典データセット
uspto-grants-2015_02
特許番号
US08952024B2

反応ノート

読み込み中…