Potassium Hydroxide → HCID 178461171, compound

HRID 2200214Notes

Reaction equation

HRID 2200214 reaction equation
[CH3:1][C@@H:2]1[CH2:6][CH2:5][C:4](=O)[CH:3]1[C:8]([O:10]CC)=O.[NH2:13][C:14]([NH2:16])=[S:15].[OH-].[K+]>C(O)C.O>[SH:15][C:14]1[N:13]=[C:8]([OH:10])[C:3]2[C@H:2]([CH3:1])[CH2:6][CH2:5][C:4]=2[N:16]=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

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) was added KOH (8.3 g, 147.9 mmol) in water (60 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. and 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. extractionextracted 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-ef6b88533d5f475986bac37cab875857
Source dataset
uspto-grants-2016_06
Patent number
US09359340B2

Reaction notes

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