1-(3,3-Dimethoxy-propyl)-5-(2-chloro-5-fluoro-pyridin-3-yl)-1H-pyrimidine-2,4-dione → HCID 58994228, compound

HRID 12702Notes

Reaction equation

HRID 12702 reaction equation
C[O:2][CH:3](OC)[CH2:4][CH2:5][N:6]1[CH:11]=[C:10]([C:12]2[C:13]([Cl:19])=[N:14][CH:15]=[C:16]([F:18])[CH:17]=2)[C:9](=[O:20])[NH:8][C:7]1=[O:21]>C1COCC1>[Cl:19][C:13]1[C:12]([C:10]2[C:9](=[O:20])[NH:8][C:7](=[O:21])[N:6]([CH2:5][CH2:4][CH:3]=[O:2])[CH:11]=2)=[CH:17][C:16]([F:18])=[CH:15][N:14]=1

Participants

3

Reactant 1

HCID 589941491-(3,3-Dimethoxy-propyl)-5-(2-chloro-5-fluoro-pyridin-3-yl)-1H-pyrimidine-2,4-dione

Product 1

HCID 58994228HCID 58994228, compoundYield 104.3%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

1-(3,3-Dimethoxy-propyl)-5-(2-chloro-5-fluoro-pyridin-3-yl)-1H-pyrimidine-2,4-dione (Prep72, 100 mg, 0.29 mmol) was dissolved in THF (3 ml) and 2N HClaq (0.5 ml) was added. The solution was stirred at room temperature for 1 hour. THF was evaporated under vacuum and the aqueous residue was lyophilized to give 90 mg of a yellow solid that was used in the next step without further purification (93% yield).

Workup

  1. addition2N HClaq (0.5 ml) was added
  2. customTHF was evaporated under vacuum

Sources & evidence

ORD record
ord-fd3ed7d83af441a785bb5c389bfe5897
Source dataset
uspto-grants-2010_06
Patent number
US07727988B2

Reaction notes

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