(1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

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Chemical Name:(1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide
CAS No.:1594129-52-8
Molecular Formula:C₂₈H₃₇N₃O₃
Molecular Weight:463.62
Hs Code.:

Synonyms:(1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

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Chemical Property of (1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

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Technology Process of (1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

There total 6 articles about (1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide 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:

: 1594131-15-3
(1R,3S)-tert-butyl (3-(1-(4-(1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcarbamoyl)cyclopentyl)carbamate

: 1594129-52-8
(1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

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

Reference yield:

: 1594129-66-4
C₂₅H₃₂N₂O₅

: 1594129-52-8
(1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 20 °C / 2250.23 Torr

2: sodium t-butanolate; chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) / 1,4-dioxane / 15 h / 20 °C / Inert atmosphere

3: ethanol / 20 °C

4: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

5: hydrogenchloride / 1,4-dioxane / 20 °C

With hydrogenchloride; chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II); palladium 10% on activated carbon; hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; sodium t-butanolate; In 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide;

Reference yield:

: tert-butyl ((S)-1-(4-((R)-pyrrolidin-3-yloxy)phenyl)ethyl)carbamate

: 1594129-52-8
(1S,3R)-3-amino-N-((S)-1-(4-((R)-1-(4-(cyclopropylmethoxy)phenyl)pyrrolidin-3-yloxy)phenyl)ethylcyclopentyl)carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium t-butanolate; chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) / 1,4-dioxane / 15 h / 20 °C / Inert atmosphere

2: ethanol / 20 °C

3: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

4: hydrogenchloride / 1,4-dioxane / 20 °C

With hydrogenchloride; chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II); O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; sodium t-butanolate; In 1,4-dioxane; ethanol; N,N-dimethyl-formamide;