tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

Base Information

Chemical Name:tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate
CAS No.:1431533-50-4
Molecular Formula:C₂₄H₂₇F₂N₃O₅
Molecular Weight:475.492
Hs Code.:

Synonyms:tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

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Chemical Property of tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

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Technology Process of tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

There total 7 articles about tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate 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:

: 1431533-49-1
tert-butyl ((2S)-1-((4-chloro-5-((4-(cyclopropylmethoxy)-2,5-difluorobenzoyl)amino)pyridin-2-yl)oxy)propan-2-yl)carbamate

: 1431533-50-4
tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

Guidance literature:: With copper(l) iodide; potassium carbonate; In N,N-dimethyl-formamide; at 160 ℃; for 4h; Microwave irradiation;

Reference yield:

: 850663-54-6
4-chloro-2-hydroxy-5-nitropyridine

: 1431533-50-4
tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.5 h / 20 °C

2.1: iron(III) chloride; iron / ethanol / 1 h / Reflux

3.1: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 0.5 h / 20 °C / Reflux

3.2: 0.5 h / 20 °C

4.1: copper(l) iodide; potassium carbonate / N,N-dimethyl-formamide / 4 h / 160 °C / Microwave irradiation

With iron(III) chloride; copper(l) iodide; oxalyl dichloride; di-isopropyl azodicarboxylate; iron; potassium carbonate; N,N-dimethyl-formamide; triphenylphosphine; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1431532-95-4
tert-butyl ((2S)-1-((4-chloro-5-nitropyridin-2-yl)oxy)propan-2-yl)carbamate

: 1431533-50-4
tert-butyl ((2S)-1-((2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)[1,3]oxazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: iron(III) chloride; iron / ethanol / 1 h / Reflux

2.1: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 0.5 h / 20 °C / Reflux

2.2: 0.5 h / 20 °C

3.1: copper(l) iodide; potassium carbonate / N,N-dimethyl-formamide / 4 h / 160 °C / Microwave irradiation

With iron(III) chloride; copper(l) iodide; oxalyl dichloride; iron; potassium carbonate; N,N-dimethyl-formamide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;