3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

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Chemical Name:3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine
CAS No.:1613332-89-0
Molecular Formula:C₂₃H₂₀ClN₅
Molecular Weight:401.898
Hs Code.:

Synonyms:3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

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Chemical Property of 3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

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Technology Process of 3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

There total 7 articles about 3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine 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: 58.0%

: 1613333-39-3
4-(4-(3-((2-chlorophenyl)ethynyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-pyrazole-1-yl)piperidine-1-carboxylic acid tert-butyl ester

: 1613332-89-0
3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

Guidance literature:: With hydrogenchloride; In dichloromethane; ethyl acetate; at 0 - 20 ℃; for 4h;

Reference yield:

: 1562305-10-5
4-(4-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylic acid tert-butyl ester

: 1613332-89-0
3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: N-iodo-succinimide / acetone / 2 h / 20 °C

2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / N,N-dimethyl-formamide / 1 h / 80 °C / Microwave irradiation

3: hydrogenchloride / dichloromethane; ethyl acetate / 4 h / 0 - 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; N-iodo-succinimide; copper(l) iodide; triethylamine; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetone;

Reference yield:

: 877399-74-1
tert-butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate

: 1613332-89-0
3-((2-chlorophenyl)ethynyl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2.3-b]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / 1,2-dimethoxyethane; water / Inert atmosphere; Reflux

2: N-iodo-succinimide / acetone / 2 h / 20 °C

3: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / N,N-dimethyl-formamide / 1 h / 80 °C / Microwave irradiation

4: hydrogenchloride / dichloromethane; ethyl acetate / 4 h / 0 - 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; N-iodo-succinimide; copper(l) iodide; sodium carbonate; triethylamine; In 1,2-dimethoxyethane; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;