Sodium Hydroxide → 2-(Methanesulfonyl)amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyrimidine

HRID 343856Notes

Reaction equation

HRID 343856 reaction equation
[CH3:1][S:2]([N:5](S(C)(=O)=O)[C:6]1[N:11]=[C:10]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15]([F:22])=[CH:14][CH:13]=2)[CH:9]=[C:8]([CH:23]([CH3:25])[CH3:24])[N:7]=1)(=[O:4])=[O:3].[OH-].[Na+]>CO>[CH3:1][S:2]([NH:5][C:6]1[N:11]=[C:10]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15]([F:22])=[CH:14][CH:13]=2)[CH:9]=[C:8]([CH:23]([CH3:25])[CH3:24])[N:7]=1)(=[O:3])=[O:4]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 218464132-(Bismethanesulfonyl)amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyrimidine

Product 1

HCID 218464172-(Methanesulfonyl)amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyrimidine

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

The 2-(bismethanesulfonyl)amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyrimidine product from Example 10B above (0.204 g) was dissolved in methanol (5 mL) and treated at room temperature with 2.5N sodium hydroxide solution (0.2 mL). The reaction mixture was stirred at room temperature for 1 hour. The mixture was partitioned between 1N hydrochloric acid and ethyl acetate. The organic layer was dried over magnesium sulfate and evaporated to dryness and recrystallized to afford 2-(methanesulfonyl)amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyrimidine as a crystalline material, m.p. 276°-276.9° C. (prior decomposition at 273° C.).

Workup

  1. customThe mixture was partitioned between 1N hydrochloric acid and ethyl acetate
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. customevaporated to dryness
  4. customrecrystallized

Sources & evidence

ORD record
ord-624506ab7866471f9b6a2cca4d1be4b8
Source dataset
uspto-grants-1999_01
Patent number
US05863924

Reaction notes

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