Water → HCID 13377359, compound
Reaction equation
[O-:1][CH2:2][CH3:3].[Na+].[Na].Cl[C:7]1[N:12]2[C:13]([CH:16]([CH3:18])[CH3:17])=[N:14][CH:15]=[C:11]2[CH:10]=[C:9]([Cl:19])[N:8]=1.O>C(O)C>[Cl:19][C:9]1[N:8]=[C:7]([O:1][CH2:2][CH3:3])[N:12]2[C:13]([CH:16]([CH3:18])[CH3:17])=[N:14][CH:15]=[C:11]2[CH:10]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of sodium ethoxide prepared in ethanol from 0.18 g (7.8 mmole) of sodium metal under nitrogen was added 1.50 g (6.52 mmole) of 5,7-dichloro-3-isopropylimidazo[1,5-c]pyrimidine (from Example 37). After three hours at room temperature the mixture was poured into 50 ml of water and extracted thrice with 30 ml portions of chlorofrom. The combined extracts were washed thrice with 40 ml portions of water, dried over magnesium sulfate and evaporated to provide crude 7-chloro-5-ethoxy-3-isopropylimidazo[1,5-c]pyrimidine.
Workup
- extractionextracted thrice with 30 ml portions of chlorofrom
- washThe combined extracts were washed thrice with 40 ml portions of water
- dry with materialdried over magnesium sulfate
- customevaporated
Sources & evidence
- ORD record
- ord-f3b037a1933542f6b2e24de71dac0ca8
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04478835
Reaction notes
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