Hydrochloric Acid → HCID 178519468, compound
Reaction equation
C1COC([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:18]2[CH:19]=[N:20][N:21]3[C:26]([OH:27])=[N:25][CH:24]=[N:23][C:22]=23)(C2C=CC=CC=2)O1.Cl.[OH2:29].CO>CC(C)=O>[C:18]([C:16]1[CH:17]=[CH:12][C:13]([C:18]2[CH:19]=[N:20][N:21]3[C:26]([OH:27])=[N:25][CH:24]=[N:23][C:22]=23)=[CH:14][CH:15]=1)(=[O:29])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:12]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 8-(4-α,α-ethylenedioxybenzylphenyl)-4-hydroxypyrazolo[1,5-a]-1,3,5-triazine (0.20 g), conc. hydrochloric acid (0.5 ml), water (1 ml), methanol (4 ml) and acetone (1 ml) is stirred at 45°-60° C. for 2 hours. After cooling, the resulting precipitate is separated by filtration, washed with water and dried to give the title compound (0.15 g).
Workup
- temperatureAfter cooling
- customthe resulting precipitate is separated by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-a3c085a5db7a49fa8b818905b8e526dd
- Source dataset
- uspto-grants-1989_04
- Patent number
- US04824834
Reaction notes
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