Isopropyl iodide → HCID 10199064, compound
Reaction equation
[CH2:1]([N:3]([CH2:15][CH3:16])[CH2:4][CH2:5][C:6]1[CH:14]=[C:13]2[C:9]([CH:10]=[CH:11][NH:12]2)=[CH:8][CH:7]=1)[CH3:2].I[CH:18]([CH3:20])[CH3:19].[H-].[Na+].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.C1(C)C=CC=CC=1>[CH2:15]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][C:6]1[CH:14]=[C:13]2[C:9]([CH:10]=[CH:11][N:12]2[CH:18]([CH3:20])[CH3:19])=[CH:8][CH:7]=1)[CH3:16]Participants
7
Procedure
Prepared from 6-(2-(Diethylamino)ethyl)-indole (14 mg, 0.0647 mmol), 2-iodopropane (44 μl, 0.259 mmol), NaH (3.1 mg, 0.129 mmol), K2CO3 (35 mg, 0.259 mmol) in 0.1 ml of DMF and 0.5 ml of toluene, according to example. Yield 8.5 mg (51%).
Sources & evidence
- ORD record
- ord-8c8d706cecf44a9a80d94e2ad160031c
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716837B1
Reaction notes
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