Triethylamine → HCID 178478732, compound
Reaction equation
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:4](Cl)[N:3]=1.[ClH:17].[I:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH2:22][NH2:23].C([N:29]([CH2:32][CH3:33])CC)C>C(O)C>[ClH:1].[ClH:17].[NH2:8][C@H:11]1[CH2:15][CH2:33][C@H:32]([NH:29][C:2]2[N:10]=[C:9]3[C:5]([N:6]=[CH:7][N:8]3[CH:11]3[CH2:15][CH2:14][CH2:13][CH2:12]3)=[C:4]([NH:23][CH2:22][C:21]3[CH:24]=[CH:25][CH:26]=[C:19]([I:18])[CH:20]=3)[N:3]=2)[CH2:13][CH2:12]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolve 2,6-dichloro-9-cyclopentylpurine (620 mg, crude), 3-iodobenzylamine hydrochloride (810 mg, 3.00 mmol) and triethylamine (835 μL, 6.00 mmol) in dry ethanol (20 mL). Heat at reflux for 15 hours, cool, and filter the solid to give the title compound as a white solid (680 mg).
Workup
- temperatureHeat
- temperatureat reflux for 15 hours
- temperaturecool
- filtrationfilter the solid
Sources & evidence
- ORD record
- ord-eaa48226350e4cfc8519326fc290f9a6
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06413974B1
Reaction notes
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