Lithium hydroxide, monohydrate → (5R)-1-{(2S)-2-((tert-butoxycarbonyl)amino)-2-cyclopentylethanoyl}-5-ethynyl-L-proline

HRID 1642658Notes

Reaction equation

HRID 1642658 reaction equation
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1)[C:10]([N:12]1[C@@H:20]([C:21]#[C:22][Si](C)(C)C)[CH2:19][CH2:18][C@H:13]1[C:14]([O:16]C)=[O:15])=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].O[Li].O>CO.O>[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH:27]1[CH2:28][CH2:29][CH2:30][CH2:31]1)[C:10]([N:12]1[C@@H:20]([C:21]#[CH:22])[CH2:19][CH2:18][C@H:13]1[C:14]([OH:16])=[O:15])=[O:11])=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

5

Reactant 2

HCID 168937Lithium hydroxide, monohydrateHCID 66756897methyl (5R)-1-{(2S)-2-((tert-butoxycarbonyl)amino)-2-cyclopentylethanoyl}-5-((trimethylsilyl)ethynyl)-L-prolinate

Product 1

HCID 86592934(5R)-1-{(2S)-2-((tert-butoxycarbonyl)amino)-2-cyclopentylethanoyl}-5-ethynyl-L-proline

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Procedure

To a stirred solution of methyl (5R)-1-{(2S)-2-((tert-butoxycarbonyl)amino)-2-cyclopentylethanoyl}-5-((trimethylsilyl)ethynyl)-L-prolinate (1.65 g, 3.66 mmol) in MeOH (10 mL) and H2O (10 mL) at room temperature was added LiOH.H2O (0.23 g, 5.49 mmol). The reaction mixture was stirred at room temperature for 16 hours and concentrated under reduced pressure. The residue was taken up in water and extracted with diethyl ether (2×). The aqueous layer was acidified to pH ˜4 by adding 4% KHSO4 dropwise. The clear solution was extracted with ethyl acetate (3×) and the combined ethyl acetate layers were washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure to provide the titled compound. MS (CI) m/e 365 (M+H)+.

Workup

  1. concentrationconcentrated under reduced pressure
  2. extractionextracted with diethyl ether (2×)
  3. additionby adding 4% KHSO4 dropwise
  4. extractionThe clear solution was extracted with ethyl acetate (3×)
  5. washthe combined ethyl acetate layers were washed with brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-82adb2a260924d07b6319e054524ea07
Source dataset
uspto-grants-2012_02
Patent number
US08119664B2

Reaction notes

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