2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

Base Information

Chemical Name:2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol
CAS No.:1608144-25-7
Molecular Formula:C₂₂H₂₄N₄O₆
Molecular Weight:440.456
Hs Code.:

Synonyms:2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

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Chemical Property of 2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

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Technology Process of 2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

There total 8 articles about 2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol 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: 91.0%

: 1608146-72-0
tert-butyl N-(5-{5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]furo[2,3-b]pyridin-2-yl}-2,2-dimethyl-1,3-dioxan-5-yl)carbamate

: 1608144-25-7
2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

Guidance literature:: With chloro-trimethyl-silane; sodium iodide; In acetonitrile; at 20 ℃; for 0.5h; Inert atmosphere;

Reference yield:

: 42182-27-4
4-cyanopyridin-2-amine

: 1608144-25-7
2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium nitrite; sulfuric acid / water / 0.5 h / 0 °C / Reflux

2.1: N-iodo-succinimide / N,N-dimethyl-formamide / 4 h / 90 °C

3.1: hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine / ethanol / 20 °C

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dimethyl sulfoxide / 2 h / 40 °C

4.2: 3 h / 110 °C / Inert atmosphere

5.1: copper(I) oxide; pyridine / 1.5 h / 110 °C / Inert atmosphere

6.1: sodium iodide; chloro-trimethyl-silane / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

With pyridine; copper(I) oxide; N-iodo-succinimide; chloro-trimethyl-silane; sulfuric acid; hydroxylamine hydrochloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium iodide; sodium nitrite; In ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 552331-00-7
4-(iodo)pyridin-2-amine

: 1608144-25-7
2-amino-2-(5-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)furo[2,3-b]pyridin-2-yl)propane-1,3-diol

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine / 0.5 h / Reflux

2.1: sodium nitrite; sulfuric acid / water / 0.5 h / 0 °C / Reflux

3.1: N-iodo-succinimide / N,N-dimethyl-formamide / 4 h / 90 °C

4.1: hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine / ethanol / 20 °C

5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dimethyl sulfoxide / 2 h / 40 °C

5.2: 3 h / 110 °C / Inert atmosphere

6.1: copper(I) oxide; pyridine / 1.5 h / 110 °C / Inert atmosphere

7.1: sodium iodide; chloro-trimethyl-silane / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

With pyridine; copper(I) oxide; N-iodo-succinimide; chloro-trimethyl-silane; sulfuric acid; hydroxylamine hydrochloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium iodide; sodium nitrite; In ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;