Water → Pregabalin

HRID 11995노트

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HRID 11995 반응식
[C:1]([C@@H:3]([CH2:8][CH:9]([CH3:11])[CH3:10])[CH2:4][C:5]([O-:7])=[O:6])#[N:2].[K+].O.[OH-].[K+].[H][H]>[Ni].C(O)(C)C>[NH2:2][CH2:1][C@@H:3]([CH2:8][CH:9]([CH3:11])[CH3:10])[CH2:4][C:5]([OH:7])=[O:6]

참가 물질

7

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온도
50 °C

실험 절차

A mixture of potassium (S)-3-cyano-5-methylhexanoate (20 g, 103.5 mmol), water (50 mL), 45% KOH (12 g), isopropanol (12 g), and Raney Nickel were shaken overnight in a Parr Shaker under 50 psi of hydrogen. The mixture was filtered, heated to approximately 50° C., treated with acetic acid (6.5 mL) and stirred overnight at room temperature. The mixture was then adjusted to slightly above pH 7 with 45% KOH and concentrated under vacuum to remove most of the isopropanol. Isopropanol (20 mL) was added to the mixture, which was then acidified with acetic acid, stirred overnight at room temperature, and filtered to give 4.3 g of (S)-3-aminomethyl-5-methylhexanoic acid as a white crystalline solid. The enantiomeric purity was determined to be 100% e.e. by preparing a derivative of (S)-3-aminomethyl-5-methylhexanoic acid using Marfey's reagent (Na-(2,4-dinitro-5-fluorophenyl)-L-alaninamide) and analyzing by HPLC on a BDS Hypersil C18 column (250×4.6 mm, 5μ) eluted with acetonitrile:1% triethylamine (pH 3) (38:62, v/v).

후처리

  1. filtrationThe mixture was filtered
  2. additiontreated with acetic acid (6.5 mL)
  3. concentrationconcentrated under vacuum
  4. customto remove most of the isopropanol
  5. additionIsopropanol (20 mL) was added to the mixture, which
  6. stirringstirred overnight at room temperature
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-bd8fc4c7ce38441fa4641ac7dc4e14fb
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07727749B2

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