N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

Base Information

Chemical Name:N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine
CAS No.:1429882-40-5
Molecular Formula:C₄₁H₅₀N₄OSi
Molecular Weight:642.96
Hs Code.:

Synonyms:N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

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Chemical Property of N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

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Technology Process of N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

There total 5 articles about N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-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: 70.0%

: 1429882-39-2
7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-2-chloro-5-trityl-5H-pyrrolo[3,2-d]pyrimidine

: 109-73-9,85404-21-3
N-butylamine

: 1429882-40-5
N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium hydroxide; XPhos; In 1,4-dioxane; water; for 12h; Reflux; Inert atmosphere;

Reference yield:

: 1119280-66-8
2-chloro-5H-pyrrolo[3,2-d]pyrimidine?

: 1429882-40-5
N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C

2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.33 h / 0 °C

2.2: 6 h

3.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C

3.2: 3 h / -78 °C

4.1: methanesulfonyl chloride; triethylamine / dichloromethane / 6 h / 20 °C

5.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium hydroxide; XPhos / 1,4-dioxane; water / 12 h / Reflux; Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; N-Bromosuccinimide; n-butyllithium; sodium hydride; methanesulfonyl chloride; triethylamine; potassium hydroxide; XPhos; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1429882-36-9
7-bromo-2-chloro-5H-pyrrolo[3,2-d]pyrimidine

: 1429882-40-5
N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohex-1-en-1-yl)-5-trityl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.33 h / 0 °C

1.2: 6 h

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C

2.2: 3 h / -78 °C

3.1: methanesulfonyl chloride; triethylamine / dichloromethane / 6 h / 20 °C

4.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium hydroxide; XPhos / 1,4-dioxane; water / 12 h / Reflux; Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; n-butyllithium; sodium hydride; methanesulfonyl chloride; triethylamine; potassium hydroxide; XPhos; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; water; mineral oil;