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Hydrochloric Acid → Pregabalin

HRID 1920499
ノート
印刷プレビュー

反応式

HRID 1920499 の反応式
C([O-])(=O)C(C(C([O-])=O)O)[OH:3].[NH2:11][CH2:12][CH:13]([CH2:22][CH:23]([CH3:25])[CH3:24])[CH2:14][C:15](N(CC)CC)=[O:16].[OH-].[Na+].[OH-].[K+].Cl>O.CO.ClCCl>[CH3:24][CH:23]([CH2:22][C@H:13]([CH2:12][NH2:11])[CH2:14][C:15]([OH:16])=[O:3])[CH3:25]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 14798Sodium HydroxideHCID 38061142,3-DihydroxybutanedioateHCID 25143769HCID 25143769、化合物

生成物 1

HCID 5486971Pregabalin

試薬・触媒・溶媒 3

HCID 887
Methanol
溶媒
HCID 962Water溶媒2 回
HCID 6344Dichloromethane溶媒

反応条件

温度
22.5 °C

実験手順

The tartarate salt of 3-aminomethyl N,N-diethyl-5-methyl hexanamide (10 grams) was dissolved in water (15 ml) and dichloromethane (25 ml) was added to it. The pH of reaction mixture was adjusted to 9-10 by addition of sodium hydroxide solution (3.0 grams in 3.0 ml of water) and stirred for 10-15 min at 20-25° C. The aqueous and organic layer was separated. The aqueous layer was extracted with dichloromethane. The solvent was distilled off from combined organic layer to obtain a residue. Potassium hydroxide (5.0 gram), water (10 ml) and methanol (10 ml) was added to the obtained residue and heated it to 70-75° C., the reaction was stirred at this temperature for 18 hours. The reaction mixture was cooled to 30° C. and the pH adjusted to 4.0 using concentrated hydrochloric acid. The reaction mixture was heated to 80° C. and stirred for 45 min and filtered. The filtrate was cooled to 5° C. The solid formed was filtered and washed with cool water. The solid was dried at 50-55° C. to yield (S)-Pregabalin.

後処理

  1. customThe pH of reaction mixture
  2. customThe aqueous and organic layer was separated
  3. extractionThe aqueous layer was extracted with dichloromethane
  4. distillationThe solvent was distilled off
  5. customto obtain a residue
  6. temperatureheated it to 70-75° C.
  7. stirringthe reaction was stirred at this temperature for 18 hours
  8. temperatureThe reaction mixture was cooled to 30° C.
  9. temperatureThe reaction mixture was heated to 80° C.
  10. stirringstirred for 45 min
  11. filtrationfiltered
  12. temperatureThe filtrate was cooled to 5° C
  13. customThe solid formed
  14. filtrationwas filtered
  15. washwashed with cool water
  16. customThe solid was dried at 50-55° C.

出典と根拠

ORDレコード
ord-d9c3b8c682124261aebbecad897ad0e1
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08168828B2

反応ノート

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