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

Base Information

Chemical Name: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
CAS No.:1610828-60-8
Molecular Formula:C₃₁H₄₁N₅O₃
Molecular Weight:531.698
Hs Code.:

Synonyms: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

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Chemical Property of 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

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Technology Process of 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

There total 3 articles about 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 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:

: 3587-60-8
Benzyloxymethyl chloride

: 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

Guidance literature:: Multi-step reaction with 3 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

With bis-triphenylphosphine-palladium(II) chloride; ammonium hydroxide; copper(l) iodide; sodium hydride; triethylamine; In 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

: 1610828-60-8
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

Guidance literature:: Multi-step reaction with 2 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

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

Reference yield:

: 4-chloro-7-iodo-2-butyl-5 pyrrolo[3,2-d]pyrimidine

: 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

Guidance literature:: Multi-step reaction with 3 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

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