Potassium Hydroxide → HCID 178461171, compound

HRID 529054Notes

Reaction equation

HRID 529054 reaction equation
[OH-].[K+].[CH3:3][C@@H:4]1[CH2:8][CH2:7][C:6](=O)[CH:5]1[C:10]([O:12]CC)=O.[NH2:15][C:16]([NH2:18])=[S:17]>O.C(O)C>[SH:17][C:16]1[N:15]=[C:10]([OH:12])[C:5]2[C@H:4]([CH3:3])[CH2:8][CH2:7][C:6]=2[N:18]=1

Participants

6

Reactant 3

HCID 14797Potassium HydroxideHCID 2723790ThioureaHCID 11052075Ethyl (2R)-2-methyl-5-oxocyclopentane-1-carboxylate

Product 1

HCID 178461171HCID 178461171, compoundYield 56%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Procedure

KOH (8.3 g, 147.9 mmol) in water (60 mL) was added to a solution of a mixture of (2R)-ethyl 2-methyl-5-oxocyclopentanecarboxylate (20 g, 117.5 mmol) and thiourea (9.2 g, 120.9 mmol) in ethanol (100 mL). The mixture was refluxed for 10 hours. After cooling, the solvent was removed, and the residue was neutralized with concentrated HCl (12 mL) at 0° C. The mixture was then extracted with DCM (3×150 mL). The solvent was removed, and the residue was purified by silica gel chromatography, eluting with hexane/ethyl acetate (2:1) to give (R)-2-mercapto-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (12 g, 56%). MS (APCI+) [M+H]+ 183.

Workup

  1. temperatureThe mixture was refluxed for 10 hours
  2. temperatureAfter cooling
  3. customthe solvent was removed
  4. customwas neutralized with concentrated HCl (12 mL) at 0° C
  5. extractionThe mixture was then extracted with DCM (3×150 mL)
  6. customThe solvent was removed
  7. customthe residue was purified by silica gel chromatography
  8. washeluting with hexane/ethyl acetate (2:1)

Sources & evidence

ORD record
ord-b4dd62cfd0d74d66a43818db0763cd25
Source dataset
uspto-grants-2016_05
Patent number
US09346805B2

Reaction notes

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