Theobromine → 6-(4-Chlorophenoxy)hexyltheobromine
Reaction equation
[NH:1]1[C:12](=[O:13])[C:11]2[N:9]([CH3:10])[CH:8]=[N:7][C:6]=2[N:4]([CH3:5])[C:2]1=[O:3].[Cl:14][C:15]1[CH:28]=[CH:27][C:18]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]Br)=[CH:17][CH:16]=1>>[Cl:14][C:15]1[CH:28]=[CH:27][C:18]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][N:1]2[C:12](=[O:13])[C:11]3[N:9]([CH3:10])[CH:8]=[N:7][C:6]=3[N:4]([CH3:5])[C:2]2=[O:3])=[CH:17][CH:16]=1Participants
3
Procedure
Theobromine and 6-(4-chlorophenoxy)hexyl bromide were reacted and treated in substantially the same manner as described in Example 9(a) to give 6-(4-chlorophenoxy)hexyltheobromine (61%).
Workup
- additiontreated in substantially the same manner
Sources & evidence
- ORD record
- ord-cc95a22ef29f492da4eeca02b62a53ea
- Source dataset
- uspto-grants-1990_07
- Patent number
- US04942143
Reaction notes
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