Hydrogen Bromide → Hydrogen Bromide
Reaction equation
[CH2:1](OC(N1CCN(C2N=CC3C(=O)N(CC)C=C(C=O)C=3N=2)CC1)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BrH:32]>C(O)(=O)C>[BrH:32].[CH2:1]([Br:32])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
Dissolved in a 25% hydrogen bromide solution of acetic acid was 0.2 g of the 2-(4-benzyloxycarbonylpiperazino)-5,6-dihydro-6-ethyl-5-oxopyrido[4,3-d]pyrimidine-8-carbaldehyde obtained in Referential Example 20. The resulting mixture was stirred at room temperature for 1 hour. Hydrogen bromide, acetic acid and resulting benzyl bromide were distilled off under reduced pressure. After neutralizing the residue with a saturated aqueous solution of sodium carbonate, the mixture was extracted with chloroform and the chloroform layer was dried with anhydrous magnesium sulfate. Chloroform was distilled off under reduced pressure to obtain 0.13 g of light yellowish crystals (yield: 95%).
Workup
- customobtained in Referential Example 20
Sources & evidence
- ORD record
- ord-b447e713bf914fa6956ac1243b9f1ce7
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04734418
Reaction notes
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