Dimethyl Sulfoxide → 2-(((3aR,4S,6R,6aS)-6-((5-amino-6-chloro-2-(propylthio)pyrimidin-4-yl)amino)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)oxy)ethanol

HRID 589813Notes

Reaction equation

HRID 589813 reaction equation
Cl[C:2]1[C:7]([NH2:8])=[C:6]([Cl:9])[N:5]=[C:4]([S:10][CH2:11][CH2:12][CH3:13])[N:3]=1.C(O)(=O)[C@@H]([C@H](C(O)=O)O)O.[NH2:24][C@H:25]1[C@@H:29]2[O:30][C:31]([CH3:34])([CH3:33])[O:32][C@@H:28]2[C@@H:27]([O:35][CH2:36][CH2:37][OH:38])[CH2:26]1.CS(C)=O.C(N(CC)CC)C>C1(C)C=CC=CC=1.O>[NH2:8][C:7]1[C:2]([NH:24][C@H:25]2[C@@H:29]3[O:30][C:31]([CH3:33])([CH3:34])[O:32][C@@H:28]3[C@@H:27]([O:35][CH2:36][CH2:37][OH:38])[CH2:26]2)=[N:3][C:4]([S:10][CH2:11][CH2:12][CH3:13])=[N:5][C:6]=1[Cl:9]

Participants

7

Conditions

Temperature
62.5 °C

Procedure

A flask was charged with 4,6-dichloro-2-(propylthio)pyrimidin-5-amine (3 g), 2-(((3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)oxy)ethanol L-tartaric acid salt (5.1 g), dimethyl sulfoxide (30 mL) and triethyl amine (7.05 g). The mixture was heated to about 60-65° C. and maintained at the same temperature for about 24 hours and completion of the reaction was monitored by TLC. After completion of reaction the mixture was cooled to 25-30° C. followed by addition of water (30 mL) and toluene (30 mL). The mixture was stirred for about 10 minutes and layers were separated. The organic layer was sequentially washed with 5% aqueous sodium carbonate solution (30 mL), 5% aqueous acetic acid solution (30 mL) and sodium chloride solution (30 mL). The organic layer was separated and subjected to complete distillation under vacuum at 55-60° C. followed by cooling to room temperature and subsequent addition of n-hexane (55 mL). The mixture was stirred for about 2-3 hours followed by isolation of solid by filtration and washing with n-hexane (10 mL). The solid isolated was subjected to drying under vacuum at 55-60° C. for 90 minutes to afford the title compound in about 60% yield having HPLC purity of about 96%.

Workup

  1. temperaturemaintained at the same temperature for about 24 hours
  2. customAfter completion of reaction the mixture
  3. temperaturewas cooled to 25-30° C.
  4. customlayers were separated
  5. washThe organic layer was sequentially washed with 5% aqueous sodium carbonate solution (30 mL), 5% aqueous acetic acid solution (30 mL) and sodium chloride solution (30 mL)
  6. customThe organic layer was separated
  7. distillationsubjected to complete distillation under vacuum at 55-60° C.
  8. temperatureby cooling to room temperature
  9. additionsubsequent addition of n-hexane (55 mL)
  10. stirringThe mixture was stirred for about 2-3 hours
  11. filtrationfollowed by isolation of solid by filtration
  12. washwashing with n-hexane (10 mL)
  13. customThe solid isolated
  14. customto drying under vacuum at 55-60° C. for 90 minutes

Sources & evidence

ORD record
ord-bfa8ad4b8ad54e0ca7db978751563ba0
Source dataset
uspto-grants-2016_01
Patent number
US09233966B2

Reaction notes

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