cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

Base Information

Chemical Name:cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate
CAS No.:1192836-42-2
Molecular Formula:C₂₂H₂₆N₄O₄S
Molecular Weight:442.539
Hs Code.:

Synonyms:cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

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Chemical Property of cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

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Technology Process of cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

There total 5 articles about cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate 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: 85.0%

: 1192836-38-6
cyclopentyl (2S,4E)-2-[(tert-butoxycarbonyl)amino]-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

: 1192836-42-2
cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; at 0 - 20 ℃; for 2.16667h;

Reference yield:

: 1021943-48-5
cyclopentyl (2S)-2-[(tert-butoxycarbonyl)amino]pent-4-enoate

: 1192836-42-2
cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

Guidance literature:: Multi-step reaction with 4 steps

1: tetra-(n-butyl)ammonium iodide; sodium hydrogencarbonate / palladium diacetate / acetonitrile / 48 h / 77 °C / Inert atmosphere

2: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / dimethyl sulfoxide / 22 h / 65 °C / Inert atmosphere

3: sodium hydrogencarbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane / 22 h / 75 °C / Inert atmosphere

4: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 2.17 h / 0 - 20 °C

With hydrogenchloride; potassium acetate; tetra-(n-butyl)ammonium iodide; sodium hydrogencarbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium diacetate; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 1192836-29-5
cyclopentyl (2S,4E)-2-[(tert-butoxycarbonyl)amino]-5-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pent-4-enoate

: 1192836-42-2
cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane / 22 h / 75 °C / Inert atmosphere

2: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 2.17 h / 0 - 20 °C

With hydrogenchloride; sodium hydrogencarbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane;