(S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

Base Information

Chemical Name:(S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole
CAS No.:1402709-66-3
Molecular Formula:C₂₇H₃₃ClN₈O
Molecular Weight:521.065
Hs Code.:

Synonyms:(S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

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Chemical Property of (S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

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Technology Process of (S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

There total 3 articles about (S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 32.0%

: 942949-34-0
5-chloro-4-[4-(5-methyl-isoxazol-3-ylmethyl)piperazin-1-yl]-3-nitro-pyridin-2-ylamine

: 1402709-68-5
(S)-4-(3,4-dimethylpiperazin-1-yl)benzaldehyde

: 1402709-66-3
(S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

Guidance literature:: With sodium dithionite; In ethanol; water; at 80 ℃; for 16h;
DOI:10.1021/jm300952s

Reference yield:

: 1152110-42-3
tert-butyl (S)-3,4-dimethylpiperazine-1-carboxylate

: 1402709-66-3
(S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane; dimethyl sulfoxide / 2 h / 120 °C

3: sodium dithionite / ethanol; water / 16 h / 80 °C

With sodium dithionite; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In ethanol; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1021/jm300952s

Reference yield:

: 147081-29-6
(S)-3-methyl-piperazine-1-carboxylic acid tert-butyl ester

: 1402709-66-3
(S)-3-((4-(6-chloro-2-(4-(3,4-dimethylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)methyl)-5-methylisoxazole

Guidance literature:: Multi-step reaction with 4 steps

1: sodium triacetoxy borohydride / tetrahydrofuran; methanol; water / 18 h

2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane; dimethyl sulfoxide / 2 h / 120 °C

4: sodium dithionite / ethanol; water / 16 h / 80 °C

With sodium triacetoxy borohydride; sodium dithionite; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1021/jm300952s