(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

Base Information

Chemical Name:(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one
CAS No.:1395322-97-0
Molecular Formula:C₁₉H₂₁FN₆O₃
Molecular Weight:400.413
Hs Code.:

Synonyms:(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

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Chemical Property of (5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

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Technology Process of (5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

There total 11 articles about (5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one 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: 23.0%

: 1395322-95-8
(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-oxohexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

: 1395322-97-0
(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

Guidance literature:: With hydroxylamine hydrochloride; sodium hydrogencarbonate; In water; at 20 ℃; for 18h;

Reference yield:

: 1395322-88-9
2-(4-amino-2-fluorophenyl)-hexahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane]

: 1395322-97-0
(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydrogencarbonate / tetrahydrofuran / 4 h / 0 - 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C

2.2: 12 h / -78 - 20 °C

3.1: triethylamine / dichloromethane / 4 h / 0 - 20 °C

4.1: sodium azide / N,N-dimethyl-formamide / 4 h / 80 °C

5.1: 48 h / Reflux

6.1: toluene-4-sulfonic acid / water; acetone / 6 h / Reflux

7.1: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol; water / 18 h / 20 °C

With n-butyllithium; sodium azide; hydroxylamine hydrochloride; sodium hydrogencarbonate; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1111/j.1747-0285.2012.01404.x

Reference yield:

: 1395322-90-3
(5R)-3-(3-fluoro-4-(tetrahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane]-2(3H)-yl)phenyl)-5-(hydroxymethyl)oxazolidin-2-one

: 1395322-97-0
(5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 4 h / 0 - 20 °C

2: sodium azide / N,N-dimethyl-formamide / 4 h / 80 °C

3: 48 h / Reflux

4: toluene-4-sulfonic acid / water; acetone / 6 h / Reflux

5: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol; water / 18 h / 20 °C

With sodium azide; hydroxylamine hydrochloride; sodium hydrogencarbonate; toluene-4-sulfonic acid; triethylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1111/j.1747-0285.2012.01404.x