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Pyridine → Methyl 6,7-dimethoxy-2-methyl-4-oxo-1,2,3,4-tetrahydroquinoline-1-carboxylate

HRID 597195
ノート
印刷プレビュー

反応式

HRID 597195 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[NH:9][CH:8]([CH3:15])[CH2:7][C:6]2=[O:16].N1C=CC=CC=1.Cl[C:24]([O:26][CH3:27])=[O:25]>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]([C:24]([O:26][CH3:27])=[O:25])[CH:8]([CH3:15])[CH2:7][C:6]2=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1049PyridineHCID 6586Methyl chloroformateHCID 214397206,7-Dimethoxy-2-methyl-2,3-dihydroquinolin-4(1H)-one

生成物 1

HCID 21439723Methyl 6,7-dimethoxy-2-methyl-4-oxo-1,2,3,4-tetrahydroquinoline-1-carboxylate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A mixture of 1.2 g. (5.45 mmol) of the quinoline product of Example 4, 792 mg. (10.7 mmol) of dry pyridine and 5.5 ml. of methylene chloride was stirred and cooled by an ice-water bath while 758 mg. (8.02 mmol) of methyl chloroformate in 1 ml. of methylene chloride was added over a 10 min. period at a rate to maintain a 10°-15° C. temperature. The ice bath was removed and the reaction allowed to stir at room temperature for 45 min. then poured onto 25 ml. of saturated sodium bicarbonate solution. The methylene chloride layer was separated and washed with 25 ml. saturated sodium bicarbonate solution and saturated sodium chloride solution, then dried over magnesium sulfate, and gravity filtered and evaporated to a yellow solid. The solid was triturated with 5 ml. anhydrous ether, filtered, and washed with minimum ether, then air dried to 1.1 g. of a yellow solid, m.p. 156°-158°. This material was dissolved in 10 ml. of hot ethyl acetate, treated with 50 mg. Darco G60, filtered and crystallized by the addition of hexane to give 727 mg. of an off-white solid, m.p. 159°-160° after drying in vacuum at 100° C (1 mm) for 24 hrs.

後処理

  1. additionA mixture of 1.2 g
  2. temperaturecooled by an ice-water bath while 758 mg
  3. temperatureto maintain a 10°-15° C. temperature
  4. customThe ice bath was removed
  5. additionthen poured onto 25 ml
  6. customThe methylene chloride layer was separated
  7. washwashed with 25 ml
  8. dry with materialsaturated sodium bicarbonate solution and saturated sodium chloride solution, then dried over magnesium sulfate, and gravity
  9. filtrationfiltered
  10. customevaporated to a yellow solid
  11. customThe solid was triturated with 5 ml
  12. filtrationanhydrous ether, filtered
  13. washwashed with minimum ether
  14. customair dried to 1.1 g
  15. dissolutionThis material was dissolved in 10 ml
  16. additionof hot ethyl acetate, treated with 50 mg
  17. filtrationDarco G60, filtered
  18. customcrystallized by the addition of hexane
  19. customto give 727 mg
  20. customof an off-white solid, m.p. 159°-160° after drying in vacuum at 100° C (1 mm) for 24 hrs

出典と根拠

ORDレコード
ord-d00be56ecbc041b58feaeec2e17771a0
出典データセット
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04013662

反応ノート

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