(R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

Base Information

Chemical Name:(R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride
CAS No.:1574538-55-8
Molecular Formula:C₂₄H₂₆N₂O₄*ClH
Molecular Weight:442.942
Hs Code.:

Synonyms:(R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

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Chemical Property of (R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

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Technology Process of (R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

There total 5 articles about (R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride 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: 37.2%

: 1574542-90-7
(R)-tert-butyl 3-(4-(3-(4-cyclopropylphenoxy)-2-oxo-2,5-dihydro-1H-pyrrol-1-yl)-2-methoxyphenoxy)pyrrolidine-1-carboxylate

: 1574538-55-8
(R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; water; at 0 - 20 ℃;

Reference yield:

: 960401-35-8
(R)-tert-butyl 3-(2-methoxy-4-nitrophenoxy)pyrrolidine-1-carboxylate

: 1574538-55-8
(R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen; 5%-palladium/activated carbon / methanol / 3 h / 20 °C

2.1: triethylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 16 h / 20 °C

3.1: sodium hydride / tetrahydrofuran / 0 - 20 °C

3.2: 0 - 20 °C

4.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 16 h / 70 °C / Inert atmosphere

5.1: hydrogenchloride / water; 1,4-dioxane / 0 - 20 °C

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; hydrogenchloride; 5%-palladium/activated carbon; hydrogen; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; water; toluene; acetonitrile;

Reference yield:

: 960401-43-8
(R)-tert-butyl 3-(4-amino-2-methoxyphenoxy)pyrrolidine-1-carboxylate

: 1574538-55-8
(R)-3-(4-cyclopropylphenoxy)-1-(3-methoxy-4-(pyrrolidin-3-yloxy)phenyl)-1H-pyrrol-2(5H)-one hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 16 h / 20 °C

2.1: sodium hydride / tetrahydrofuran / 0 - 20 °C

2.2: 0 - 20 °C

3.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 16 h / 70 °C / Inert atmosphere

4.1: hydrogenchloride / water; 1,4-dioxane / 0 - 20 °C

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; hydrogenchloride; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; 1,4-dioxane; water; toluene; acetonitrile;