2-(5-chloro-2-((3-(4-methylpiperazin-1-yl)propyl)amino)pyrimidin-4-yl)-N-cyclopropylbenzo[b]thiophene-4-carboxamide trihydrochloride → 2-{5-Chloro-2-[3-(4-methylpiperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid methoxyamide tri-hydrochloride
Reaction equation
[ClH:1].Cl.Cl.C1([NH:7][C:8]([C:10]2[C:18]3[CH:17]=[C:16]([C:19]4[C:24]([Cl:25])=[CH:23][N:22]=[C:21]([NH:26][CH2:27][CH2:28][CH2:29][N:30]5[CH2:35][CH2:34][N:33]([CH3:36])[CH2:32][CH2:31]5)[N:20]=4)[S:15][C:14]=3[CH:13]=[CH:12][CH:11]=2)=[O:9])CC1.[Cl:37]C1N=C(C2SC3C=CC=C([C:53](O)=[O:54])C=3C=2)C(Cl)=CN=1>>[ClH:25].[ClH:37].[ClH:1].[CH3:53][O:54][NH:7][C:8]([C:10]1[C:18]2[CH:17]=[C:16]([C:19]3[C:24]([Cl:25])=[CH:23][N:22]=[C:21]([NH:26][CH2:27][CH2:28][CH2:29][N:30]4[CH2:35][CH2:34][N:33]([CH3:36])[CH2:32][CH2:31]4)[N:20]=3)[S:15][C:14]=2[CH:13]=[CH:12][CH:11]=1)=[O:9]Participants
3
Reactant 2
Product 1
Procedure
Using the method of 2-{5-chloro-2-[3-(4-methylpiperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride, the title compound is synthesized from 2-(2,5-dichloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid and isolated as a yellow solid. ES+(m/z) 475 (35Cl) and 477 (37Cl) [M(free base)+H].
Workup
- customisolated as a yellow solid
Sources & evidence
- ORD record
- ord-4bf204515fad4f36a2b1abdce9c49b43
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07547691B2
Reaction notes
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