N,N-Diethyl-1,4-butanediamine → N-[2-(3-Cyano-1H-indol-5-yl)ethyl]-4-[2-(4-diethylaminobutylamino)pyrimidin-4-yl]benzamide
Reaction equation
[CH2:1]([N:3]([CH2:9][CH3:10])[CH2:4][CH2:5][CH2:6][CH2:7][NH2:8])[CH3:2].[C:11]([C:13]1[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([CH2:22][CH2:23][NH:24][C:25](=[O:39])[C:26]3[CH:31]=[CH:30][C:29]([C:32]4[CH:37]=[CH:36][N:35]=[C:34](Cl)[N:33]=4)=[CH:28][CH:27]=3)[CH:20]=2)[NH:15][CH:14]=1)#[N:12]>>[C:11]([C:13]1[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([CH2:22][CH2:23][NH:24][C:25](=[O:39])[C:26]3[CH:31]=[CH:30][C:29]([C:32]4[CH:37]=[CH:36][N:35]=[C:34]([NH:8][CH2:7][CH2:6][CH2:5][CH2:4][N:3]([CH2:9][CH3:10])[CH2:1][CH3:2])[N:33]=4)=[CH:28][CH:27]=3)[CH:20]=2)[NH:15][CH:14]=1)#[N:12]Participants
3
Procedure
Using 4-diethylaminobutylamine (reference example 93h) and N-[2-(3-Cyano-1H-indol-5-yl)-ethyl]-4-[2-chloro-pyrimidin-4-yl]-benzamide (reference example 1az) as substrates. MS (ion spray) m/z 510 (M+H)+.
Sources & evidence
- ORD record
- ord-503acb00c5884f77aab06a086c1e2ca9
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06541505B1
Reaction notes
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