(3-Bromopropyl)diethylamine hydrobromide → 7,7-Dimethyl-2-cyclopropyl-5-(3-diethylamino-propyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione
Reaction equation
Cl.[CH3:2][C:3]1([CH3:21])[C:12](=[O:13])[CH:11]2[C:6](=[C:7]3[N:17]=[C:16]([CH:18]4[CH2:20][CH2:19]4)[N:15]=[C:8]3[C:9](=[O:14])[CH2:10]2)[CH:5]=[N:4]1.Br.[CH2:23]([N:25]([CH2:30][CH3:31])[CH2:26][CH2:27][CH2:28]Br)[CH3:24]>>[CH3:2][C:3]1([CH3:21])[C:12](=[O:13])[CH:11]2[C:6](=[C:7]3[N:17]=[C:16]([CH:18]4[CH2:19][CH2:20]4)[N:15]=[C:8]3[C:9](=[O:14])[CH:10]2[CH2:28][CH2:27][CH2:26][N:25]([CH2:30][CH3:31])[CH2:23][CH3:24])[CH:5]=[N:4]1Participants
3
Procedure
Prepared analogous to Example 23 from 2.45 gm of 7,7-dimethyl-2-cyclopropyl-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione hydrochloride and 2.3 gm of 3-diethylamino-propyl bromide hydrobromide. The crude product was purified by chromatography on a silicagel column (eluant: chloroform with increasing content of acetone).
Workup
- customThe crude product was purified by chromatography on a silicagel column (eluant: chloroform with increasing content of acetone)
Sources & evidence
- ORD record
- ord-e2ef9d45951040e392ad9e691da19a6c
- Source dataset
- uspto-grants-1979_11
- Patent number
- US04176184
Reaction notes
Loading…