potassium (S)-3-cyano-5-methylhexanoate → Pregabalin

HRID 1667393Notes

Reaction equation

HRID 1667393 reaction equation
[K+].[C:2]([C@@H:4]([CH2:9][CH:10]([CH3:12])[CH3:11])[CH2:5][C:6]([O-:8])=[O:7])#[N:3]>[Ni].O>[CH3:12][CH:10]([CH2:9][C@H:4]([CH2:2][NH2:3])[CH2:5][C:6]([OH:8])=[O:7])[CH3:11]

Participants

4

Conditions

Temperature
70 °C

Procedure

A hydrogenator (12000 L) is charged with water (942.1 L) and with the reaction mixture from Example 12, which contains (S)-3-cyano-5-methyl-hexanoic acid potassium salt (Formula 26, 4122.9 L). A Raney nickel suspension (219.6 kg, 50% w/w in H2O) is added. The hydrogenation is conducted under 50 psig at 35° C. After 6 h, the Raney nickel is filtered and the resulting filtrate is transferred to a reactor (16000 L) for crystallization. After adding H2O (1098 L), the pH of the solution is adjusted to 7.0-7.5 using HOAc (864.7 kg). The resulting precipitate is filtered and washed once with H2O (549 L) and twice with IPA (2,586 L each). The solid is recrystallized with IPA (12296 L) and H2O (6148 L). The mixture is heated to 70° C. and subsequently cooled to 4° C. After 5-10 h, the crystalline solid is filtered, washed with IPA (5724 L), and dried in a vacuum oven at 45° C. for 24 h to give pregabalin as a white crystalline solid (1431 kg, 30.0% overall yield, 99.5% purity and 99.75% ee).

Workup

  1. customis conducted under 50 psig at 35° C
  2. filtrationthe Raney nickel is filtered
  3. customthe resulting filtrate is transferred to a reactor
  4. custom(16000 L) for crystallization
  5. additionAfter adding H2O (1098 L)
  6. filtrationThe resulting precipitate is filtered
  7. washwashed once with H2O (549 L) and twice with IPA (2,586 L each)
  8. customThe solid is recrystallized with IPA (12296 L) and H2O (6148 L)
  9. temperaturesubsequently cooled to 4° C
  10. waitAfter 5-10 h
  11. filtrationthe crystalline solid is filtered
  12. washwashed with IPA (5724 L)
  13. customdried in a vacuum oven at 45° C. for 24 h

Sources & evidence

ORD record
ord-1538b19241684ca2b2246af957873e51
Source dataset
uspto-grants-2011_10
Patent number
US08044227B2

Reaction notes

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