Trifluoroacetic acid → Ethyl 6-(4-fluorobenzyl)-4-hydroxy-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxylate

HRID 1817301ノート

反応式

HRID 1817301 の反応式
C(O[C:6]1[O:10][C:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N:8][CH:7]=1)CCC.[F:16][C:17]1[CH:30]=[CH:29][C:20]([CH2:21][N:22]2[CH2:27][CH2:26][CH:25]=[CH:24][C:23]2=[O:28])=[CH:19][CH:18]=1.FC(F)(F)C(O)=O>CCOCC>[F:16][C:17]1[CH:18]=[CH:19][C:20]([CH2:21][N:22]2[CH2:27][CH2:26][C:25]3[C:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N:8][CH:7]=[C:6]([OH:10])[C:24]=3[C:23]2=[O:28])=[CH:29][CH:30]=1

参加物

5

反応物 3

HCID 6422Trifluoroacetic acidHCID 66996945Ethyl 5-butoxy-1,3-oxazole-2-carboxylateHCID 690647451-(4-Fluorobenzyl)-5,6-dihydropyridin-2-(1H)-one

生成物 1

HCID 69061030Ethyl 6-(4-fluorobenzyl)-4-hydroxy-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxylate

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
130 °C

実験手順

In a heavy walled round bottom flask with screw top were combined ethyl 5-butoxy-1,3-oxazole-2-carboxylate (2.53 g, 11.88 mmol) and 1-(4-fluorobenzyl)-5,6-dihydropyridin-2-(1H)-one (1.22 g, 5.94 mmol; see Example 1, Step 3) and trifluoroacetic acid (0.46 mL, 5.94 mmol). The vessel was sealed and placed in an oil bath heated to 130° C. The reaction mixture was stirred for 3 days. The dark brown reaction mixture was cooled and a crystalline precipitate formed. The mixture was diluted with ether and the solids collected by filtration and washed with ether to give the product as tan shiny plates. Further product can be obtained by evaporating the mother liquor, adding more trifluoroacetic acid and re-heating the mixture.

後処理

  1. customIn a heavy walled round bottom flask with screw top were combined
  2. customThe vessel was sealed
  3. customplaced in an oil bath
  4. temperatureThe dark brown reaction mixture was cooled
  5. customa crystalline precipitate formed
  6. filtrationthe solids collected by filtration
  7. washwashed with ether
  8. customto give the product as tan shiny plates
  9. customFurther product can be obtained
  10. customby evaporating the mother liquor
  11. additionadding more trifluoroacetic acid
  12. temperaturere-heating the mixture

出典と根拠

ORDレコード
ord-0ce00a3796854952bb87784b3e95aed3
出典データセット
uspto-grants-2009_10
特許番号
US07598264B2

反応ノート

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