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 589814Notes

Reaction equation

HRID 589814 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
100 °C

Procedure

A flask was charged with 4,6-dichloro-2-(propylthio)pyrimidin-5-amine (50 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 (84.83 g), dimethyl sulfoxide (500 mL) and triethyl amine (127.5 g). The mixture was heated to about 95-105° C. and maintained at the same temperature for about 10-12 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 (1000 mL) and toluene (600 mL). The mixture was stirred for about 10 minutes and layers were separated. The organic layer was sequentially washed with 20% aqueous sodium carbonate solution (1000 mL), 20% aqueous acetic acid solution (1000 mL) and water (700 mL). The organic layer was separated and subjected to complete distillation under vacuum at 60-65° C. followed by cooling to room temperature and subsequent addition of n-hexane (800 mL). The mixture was stirred for about 9 hours at room temperature followed by isolation of solid by filtration and washing with n-hexane (100 mL). The solid isolated was subjected to drying under vacuum at 55-60° C. for about 5 hours to afford the title compound in about 84% yield having HPLC purity of about 98%.

Workup

  1. temperaturemaintained at the same temperature for about 10-12 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 20% aqueous sodium carbonate solution (1000 mL), 20% aqueous acetic acid solution (1000 mL) and water (700 mL)
  6. customThe organic layer was separated
  7. distillationsubjected to complete distillation under vacuum at 60-65° C.
  8. temperatureby cooling to room temperature
  9. additionsubsequent addition of n-hexane (800 mL)
  10. stirringThe mixture was stirred for about 9 hours at room temperature
  11. filtrationfollowed by isolation of solid by filtration
  12. washwashing with n-hexane (100 mL)
  13. customThe solid isolated
  14. customto drying under vacuum at 55-60° C. for about 5 hours

Sources & evidence

ORD record
ord-233d7879ce5e433ca150f57a281f2fe0
Source dataset
uspto-grants-2016_01
Patent number
US09233966B2

Reaction notes

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