(S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate

Base Information

Chemical Name:(S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate
CAS No.:1085706-44-0
Molecular Formula:C₁₇H₂₁IN₄O₂
Molecular Weight:440.284
Hs Code.:

Synonyms:(S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate

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Chemical Property of (S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate

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Technology Process of (S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate

There total 2 articles about (S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)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: 24.0%

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 4-iodobenzimidohydrazide

: 1085706-44-0
(S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate

Guidance literature:: 1-(tert-butoxycarbonyl)-L-proline; With triethylamine; isobutyl chloroformate; In tetrahydrofuran; at -10 ℃; for 0.333333h;

4-iodobenzimidohydrazide; In tetrahydrofuran; for 2h;

In xylene; at 185 ℃; for 0.5h;

Reference yield:

: 3058-39-7
4-iodobenzonitrile

: 1085706-44-0
(S)-tert-butyl 2-(5-(4-iodophenyl)-4H-1,2,4-triazol-3-yl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / methanol / 48.67 h / 0 °C

1.2: 1 h / 20 °C

2.1: triethylamine; isobutyl chloroformate / tetrahydrofuran / 0.33 h / -10 °C

2.2: 2 h

2.3: 0.5 h / 185 °C

With hydrogenchloride; triethylamine; isobutyl chloroformate; In tetrahydrofuran; methanol;

Reference yield: 78.0%

: 1208008-44-9
(S)-2-(5-ethynyl-1H-benzoimidazol-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

: 1085706-44-0
(S)-tert-butyl 2-(3-(4-iodophenyl)-1H-1,2,4-triazol-5-yl)pyrrolidine-1-carboxylate

: 1242087-56-4
C₃₅H₄₁N₇O₄

Guidance literature:: With copper(l) iodide; triethylamine; trans-bis(triphenylphosphine)palladium dichloride; In acetonitrile; at 50 ℃; for 3h; Inert atmosphere;