Hydrochloric Acid → HCID 19689240, compound
Reaction equation
[CH2:1]([N:8]1[C:17](=[O:18])[C:16]2[N:15](COCC)[CH:14]=[N:13][C:12]=2[N:11]([CH3:23])[C:9]1=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:24]>>[ClH:24].[CH2:1]([N:8]1[C:17](=[O:18])[C:16]2[NH:15][CH:14]=[N:13][C:12]=2[N:11]([CH3:23])[C:9]1=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Conditions
- Temperature
- 60 °C
Procedure
The unpurified 1-benzyl-7-ethoxymethyl-3-methylxanthine was treated with 1000 ml of 5N hydrochloric acid and stirred at 60° C. for 6 hours. The precipitated solid was filtered off with suction, washed with ethanol and dried under reduced pressure (164 g). It was possible from the mother liquor, after concentrating to approximately 50%, to isolate a further 35 g of the desired product.
Workup
- filtrationThe precipitated solid was filtered off with suction
- washwashed with ethanol
- customdried under reduced pressure (164 g)
- concentrationafter concentrating to approximately 50%
Sources & evidence
- ORD record
- ord-3a7e91768d4c487cad45cb6ac939a6f7
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05728686
Reaction notes
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