2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

Base Information

Chemical Name:2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid
CAS No.:1335138-73-2
Molecular Formula:C₁₇H₂₈N₄O₂
Molecular Weight:320.435
Hs Code.:

Synonyms:2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

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Chemical Property of 2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

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Technology Process of 2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

There total 8 articles about 2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid 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:

: ethyl 2-{(3S)-3-[(tert-butoxycarbonyl)amino]pyrrolidin-1-yl}-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionate

: 1335138-73-2
2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

Guidance literature:: With hydrogenchloride; water; for 10h; Reflux;

Reference yield:

: 1335139-08-6
1-(trans-4-methylcyclohexyl)-1H-imidazole-4-carbaldehyde

: 1335138-73-2
2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran / 1 h / 0 °C

1.2: 1 h / 0 °C

2.1: palladium 10% on activated carbon; hydrogen; water / ethanol / 5 h / 55 °C / 760.05 Torr

3.1: lithium hexamethyldisilazane / tetrahydrofuran; hexane / 1 h / -78 °C

3.2: 0.5 h / -78 °C

4.1: N-Bromosuccinimide / tetrahydrofuran; hexane / 1 h / -78 °C

4.2: 2 h / -78 - 20 °C

4.3: 12 h / 50 °C

5.1: water; hydrogenchloride / 10 h / Reflux

With hydrogenchloride; N-Bromosuccinimide; palladium 10% on activated carbon; water; hydrogen; sodium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; hexane; 1.1: |Wittig-Horner Reaction / 1.2: |Wittig-Horner Reaction;

Reference yield:

: 1335139-86-0
ethyl 3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionate

: 1335138-73-2
2-[(3S)-3-aminopyrrolidin-1-yl]-3-[1-(trans-4-methylcyclohexyl)-1H-imidazol-4-yl]propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran; hexane / 1 h / -78 °C

1.2: 0.5 h / -78 °C

2.1: N-Bromosuccinimide / tetrahydrofuran; hexane / 1 h / -78 °C

2.2: 2 h / -78 - 20 °C

2.3: 12 h / 50 °C

3.1: water; hydrogenchloride / 10 h / Reflux

With hydrogenchloride; N-Bromosuccinimide; water; lithium hexamethyldisilazane; In tetrahydrofuran; hexane;