5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Base Information

Chemical Name:5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine
CAS No.:1610828-61-9
Molecular Formula:C₂₆H₃₃N₅O
Molecular Weight:431.581
Hs Code.:

Synonyms:5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

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Chemical Property of 5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

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Technology Process of 5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

There total 5 articles about 5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine 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:

: 1610828-60-8
tert-butyl 4-(3-(4-amino-5-((benzyloxy)methyl)-2-butyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)prop-2-yn-1-yl)piperidine-1-carboxylate

: 1610828-61-9
5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 20 ℃; for 15h;

Reference yield:

: 3587-60-8
Benzyloxymethyl chloride

: 1610828-61-9
5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Cooling with ice

1.2: 20 °C

2.1: ammonium hydroxide / isopropyl alcohol / 3 h / 120 °C / Microwave irradiation

3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

3.2: 0.67 h / 55 °C

4.1: hydrogenchloride / 1,4-dioxane; methanol / 15 h / 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; ammonium hydroxide; copper(l) iodide; sodium hydride; triethylamine; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;

Reference yield:

: 1610828-58-4
5-((benzyloxy)methyl)-2-butyl-4-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine

: 1610828-61-9
5-((benzyloxy)methyl)-2-butyl-7-(3-(piperidin-4-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium hydroxide / isopropyl alcohol / 3 h / 120 °C / Microwave irradiation

2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2.2: 0.67 h / 55 °C

3.1: hydrogenchloride / 1,4-dioxane; methanol / 15 h / 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; ammonium hydroxide; copper(l) iodide; triethylamine; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; isopropyl alcohol;