Phosphorus oxychloride → (R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine

HRID 1806065Notes

Reaction equation

HRID 1806065 reaction equation
[CH3:1][C@H:2]1[C:10]2[C:9](O)=[N:8][CH:7]=[N:6][C:5]=2[CH2:4][CH2:3]1.O=P(Cl)(Cl)[Cl:14]>>[Cl:14][C:9]1[C:10]2[C@H:2]([CH3:1])[CH2:3][CH2:4][C:5]=2[N:6]=[CH:7][N:8]=1

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178461168HCID 178461168, compound

Product 1

HCID 59670769(R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidineYield 44%

Procedure

The solution of (R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (2.08 g, 13.9 mmol) in POCl3 (10 ml) was refluxed for 2 hours. After cooling, the excess POCl3 was evaporated and the residue was dissolved in CH2Cl2 (50 ml) and was neutralized with saturated NaHCO3. The aqueous phase was extracted with CH2Cl2. The organic phase was dried and concentrated. The residue purified on silica gel (20% EtOAc in hexanes) to afford the title compound (1.0 g, 44% yield).

Workup

  1. temperatureAfter cooling
  2. customthe excess POCl3 was evaporated
  3. dissolutionthe residue was dissolved in CH2Cl2 (50 ml)
  4. extractionThe aqueous phase was extracted with CH2Cl2
  5. customThe organic phase was dried
  6. concentrationconcentrated
  7. customThe residue purified on silica gel (20% EtOAc in hexanes)

Sources & evidence

ORD record
ord-1e01a61d52f94f02acb7c56767ddb1dc
Source dataset
uspto-grants-2013_01
Patent number
US08354540B2

Reaction notes

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