(2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

Base Information

Chemical Name:(2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
CAS No.:1256390-88-1
Molecular Formula:C₂₀H₂₆BrN₃O₃
Molecular Weight:436.349
Hs Code.:

Synonyms:(2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

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Chemical Property of (2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

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Technology Process of (2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

There total 7 articles about (2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate 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:

: 40216-83-9
L-4-hydroxyproline methyl ester hydrochloride

: 1256390-88-1
(2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: triethylamine / dichloromethane / 20 °C

2: Dess-Martin periodane / dichloromethane / 4 h / 0 - 20 °C

3: potassium carbonate / 0 - 20 °C

4: palladium on activated charcoal; hydrogen; magnesium oxide / methanol / 2 h / 20 °C

5: Dess-Martin periodane; lithium hydroxide / tetrahydrofuran; methanol / 2 h / 20 °C

6: triethylamine / dichloromethane / 3 h / 20 °C

7: ammonium acetate / toluene

With palladium on activated charcoal; ammonium acetate; hydrogen; magnesium oxide; potassium carbonate; Dess-Martin periodane; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; toluene;

Reference yield:

: 74844-91-0
1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate

: 1256390-88-1
(2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: Dess-Martin periodane / dichloromethane / 4 h / 0 - 20 °C

2: potassium carbonate / 0 - 20 °C

3: palladium on activated charcoal; hydrogen; magnesium oxide / methanol / 2 h / 20 °C

4: Dess-Martin periodane; lithium hydroxide / tetrahydrofuran; methanol / 2 h / 20 °C

5: triethylamine / dichloromethane / 3 h / 20 °C

6: ammonium acetate / toluene

With palladium on activated charcoal; ammonium acetate; hydrogen; magnesium oxide; potassium carbonate; Dess-Martin periodane; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; toluene;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1256390-88-1
(2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: triethylamine / dichloromethane / 20 °C

2: Dess-Martin periodane / dichloromethane / 4 h / 0 - 20 °C

3: potassium carbonate / 0 - 20 °C

4: palladium on activated charcoal; hydrogen; magnesium oxide / methanol / 2 h / 20 °C

5: Dess-Martin periodane; lithium hydroxide / tetrahydrofuran; methanol / 2 h / 20 °C

6: triethylamine / dichloromethane / 3 h / 20 °C

7: ammonium acetate / toluene

With palladium on activated charcoal; ammonium acetate; hydrogen; magnesium oxide; potassium carbonate; Dess-Martin periodane; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; toluene;