Lithium Hydroxide → HCID 58465352, compound

HRID 2192413Notes

Reaction equation

HRID 2192413 reaction equation
[OH-].[Li+].[CH3:3][C@H:4]1[C:12]2[C:11]([C:13]3[S:17][C:16]([C:18]([O-:20])=[O:19])=[CH:15][CH:14]=3)=[N:10][CH:9]=[N:8][C:7]=2[C@H:6]([O:21]C(=O)C2C=CC([N+]([O-])=O)=CC=2)[CH2:5]1>C1COCC1.O>[OH:21][C@H:6]1[C:7]2[N:8]=[CH:9][N:10]=[C:11]([C:13]3[S:17][C:16]([C:18]([OH:20])=[O:19])=[CH:15][CH:14]=3)[C:12]=2[C@H:4]([CH3:3])[CH2:5]1

Participants

5

Reactant 2

HCID 3939Lithium HydroxideHCID 67436393HCID 67436393, compound

Product 1

HCID 58465352HCID 58465352, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

Lithium hydroxide (6 mg, 0.146 mmol) was added to a solution of 5-((5R,7R)-5-methyl-7-(4-nitrobenzoyloxy)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)thiophene-2-carboxylate (32 mg, 0.073 mmol) in THF (0.5 mL) and water (0.5 mL). The reaction mixture was stirred at room temperature for 1 hour. LC-MS of the reaction mixture showed no more starting material. THF was removed under reduced pressure, and 1N HCl (5 mL) was added. The reaction mixture was extracted with EtOAc (3×5 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to give 5-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)thiophene-2-carboxylic acid. The crude mixture was used directly in the next step without further purification.

Workup

  1. customTHF was removed under reduced pressure, and 1N HCl (5 mL)
  2. additionwas added
  3. extractionThe reaction mixture was extracted with EtOAc (3×5 mL)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-4c6af6dfe73b43a1852120d496ff4b17
Source dataset
uspto-grants-2012_12
Patent number
US08329709B2

Reaction notes

Loading…