tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

Base Information

Chemical Name:tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate
CAS No.:1422429-03-5
Molecular Formula:C₂₁H₂₈BrN₃O₂
Molecular Weight:434.376
Hs Code.:

Synonyms:tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

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Chemical Property of tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

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Technology Process of tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

There total 4 articles about tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate 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: 26.0%

: 1422429-02-4
2-(4-bromophenyl)-2-oxoethyl (1S,2S)-2-((tert-butoxycarbonyl)(ethyl)amino)cyclopentanecarboxylate

: 1422429-03-5
tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

Guidance literature:: With ammonium acetate; In toluene; at 110 ℃; for 18h;

Reference yield:

: 1422428-99-6
ethyl (1S,2S)-2-(ethylamino)cyclopentanecarboxylate

: 1422429-03-5
tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydrogencarbonate / 1,4-dioxane; water / 16 h / 20 - 40 °C

2: lithium hydroxide; water / tetrahydrofuran; ethanol / 4 h / 20 - 40 °C

3: N-ethyl-N,N-diisopropylamine / 3 h / 20 - 40 °C

4: ammonium acetate / toluene / 18 h / 110 °C

With ammonium acetate; water; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; water; toluene;

Reference yield:

: 1609100-30-2,752181-59-2
ethyl (1S,2S)-2-aminocyclopentanecarboxylate

: 1422429-03-5
tert-butyl ((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)(ethyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetic acid / tetrahydrofuran / 1 h / 20 - 40 °C

1.2: 16 h / 20 - 40 °C

2.1: sodium hydrogencarbonate / 1,4-dioxane; water / 16 h / 20 - 40 °C

3.1: lithium hydroxide; water / tetrahydrofuran; ethanol / 4 h / 20 - 40 °C

4.1: N-ethyl-N,N-diisopropylamine / 3 h / 20 - 40 °C

5.1: ammonium acetate / toluene / 18 h / 110 °C

With ammonium acetate; water; sodium hydrogencarbonate; acetic acid; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; water; toluene;