tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

Base Information

Chemical Name:tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate
CAS No.:1610698-26-4
Molecular Formula:C₂₉H₂₉N₅O₃
Molecular Weight:495.581
Hs Code.:

Synonyms:tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

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Chemical Property of tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

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Technology Process of tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

There total 5 articles about tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-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: 39.0%

: 1610698-61-7
tert-butyl (R)-3-(4-amino-5-(4-phenoxyphenyl)-6-((trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

: 1610698-26-4
tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

Guidance literature:: With methanol; potassium fluoride; at 20 ℃; for 0.5h;

Reference yield:

: 1610697-81-8
tert-butyl (R)-3-(4-amino-6-bromo-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

: 1610698-26-4
tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 80 °C / Inert atmosphere; Microwave irradiation; Sealed tube

2: potassium fluoride; methanol / 0.5 h / 20 °C

With methanol; bis-triphenylphosphine-palladium(II) chloride; potassium fluoride; copper(l) iodide; triethylamine; In toluene;

Reference yield:

: 1272668-51-5
(R)-3-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylic acid tert-butyl ester

: 1610698-26-4
tert-butyl (R)-3-(4-amino-6-ethynyl-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: ammonium hydroxide / 1,4-dioxane / 0.83 h / 120 °C / Microwave irradiation; Sealed tube

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / 1,2-dimethoxyethane; water / 90 °C / Inert atmosphere

3: N-Bromosuccinimide / dichloromethane / 0.5 h / 20 °C

4: copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 80 °C / Inert atmosphere; Microwave irradiation; Sealed tube

5: potassium fluoride; methanol / 0.5 h / 20 °C

With methanol; bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; ammonium hydroxide; N-Bromosuccinimide; copper(l) iodide; sodium carbonate; triethylamine; In 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; water; toluene;