Lithium hydroxide, monohydrate → HCID 68931117, compound

HRID 1926687Notes

Reaction equation

HRID 1926687 reaction equation
[CH3:1][C@@H:2]1[CH2:7][N:6]([C@@H:8]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:9]2[CH:14]=[CH:13][C:12]([C:15]#[C:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11][CH:10]=2)[CH2:5][CH2:4][N:3]1[CH2:29][C:30]([O:32]C(C)(C)C)=[O:31].O.[OH-].[Li+]>C1COCC1.CO.O>[CH3:1][C@@H:2]1[CH2:7][N:6]([C@@H:8]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:9]2[CH:10]=[CH:11][C:12]([C:15]#[C:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:13][CH:14]=2)[CH2:5][CH2:4][N:3]1[CH2:29][C:30]([OH:32])=[O:31]

Participants

4

Procedure

To a solution of tert-butyl 2-((R)-2-methyl-4-((S)-phenyl(4-(2-phenylethynyl)phenyl)-methyl)piperazin-1-yl)acetate (320 mg, 0.666 mmol) in THF/MeOH/H2O=5:5:1 (5.5 mL) was added lithium hydroxide monohydrate (279 mg, 6.658 mmol) and the resulting solution was stirred overnight. The solvent was evaporated to dryness under high vacuum and the residue was diluted with water, adjusted pH=5, extracted with DCM, dried over Na2SO4, filtered and evaporated to dryness. The residue was loaded onto flash column (SiO2, DCM to DCM/MeOH=100:5 to 100:10 to 100:15 to 100:20) to give 2-((R)-2-methyl-4-((S)-phenyl(4-(2-phenylethynyl)phenyl)methyl)piperazin-1-yl)acetic acid (240 mg) as a white solid.

Workup

  1. customThe solvent was evaporated to dryness under high vacuum
  2. additionthe residue was diluted with water, adjusted pH=5
  3. extractionextracted with DCM
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated to dryness

Sources & evidence

ORD record
ord-a321bf9674a54c4ab842bb1e541bdb0a
Source dataset
uspto-grants-2012_05
Patent number
US08183244B2

Reaction notes

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