3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

Base Information

Chemical Name:3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide
CAS No.:1374974-08-9
Molecular Formula:C₁₇H₂₀F₂N₆O₂
Molecular Weight:378.382
Hs Code.:

Synonyms:3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

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Chemical Property of 3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

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Technology Process of 3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

There total 4 articles about 3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide 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:

: 1374969-72-8
tert-butyl (1S,2R)-2-(5-cyano-3-fluoro-6-(5-fluoropyridin-3-ylamino)pyridin-2-ylamino)cyclohexylcarbamate

: 1374974-08-9
3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

Guidance literature:: tert-butyl (1S,2R)-2-(5-cyano-3-fluoro-6-(5-fluoropyridin-3-ylamino)pyridin-2-ylamino)cyclohexylcarbamate; With dihydrogen peroxide; potassium hydroxide; In methanol; dimethyl sulfoxide; at 20 ℃; for 0.666667h;

With 3-chloro-benzenecarboperoxoic acid; In methanol; dimethyl sulfoxide; at 20 ℃;

Reference yield:

: 82671-02-1
2,6-dichloro-5-fluoro-pyridine-3-carbonitrile

: 1374974-08-9
3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 80 °C

2.1: caesium carbonate / bis(dibenzylideneacetone)-palladium⁽⁰⁾; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene / toluene / 0.05 h / 110 °C / Inert atmosphere

3.1: potassium hydroxide; dihydrogen peroxide / dimethyl sulfoxide; methanol / 0.67 h / 20 °C

3.2: 20 °C

With dihydrogen peroxide; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium hydroxide; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In 1-methyl-pyrrolidin-2-one; methanol; dimethyl sulfoxide; toluene;

Reference yield:

: 365996-30-1
tert-butyl ((1S,2R)-2-aminocyclohexyl)carbamate

: 1374974-08-9
3-(6-((1R,2S)-2-aminocyclohexylamino)-3-carbamoyl-5-fluoropyridin-2-ylamino)-5-fluoropyridine-1-oxide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 80 °C

2.1: caesium carbonate / bis(dibenzylideneacetone)-palladium⁽⁰⁾; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene / toluene / 0.05 h / 110 °C / Inert atmosphere

3.1: potassium hydroxide; dihydrogen peroxide / dimethyl sulfoxide; methanol / 0.67 h / 20 °C

3.2: 20 °C

With dihydrogen peroxide; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium hydroxide; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In 1-methyl-pyrrolidin-2-one; methanol; dimethyl sulfoxide; toluene;