tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

Base Information

Chemical Name:tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate
CAS No.:901309-40-8
Molecular Formula:C₂₄H₂₅BrF₃N₃O₃S
Molecular Weight:572.446
Hs Code.:

Synonyms:tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

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Chemical Property of tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

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Technology Process of tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

There total 8 articles about tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)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: 87.0%

: 901309-22-6
5-bromo-N-{2-[2-(tert-butyl)phenoxy]pyridin-3-yl}-4-(trifluoromethyl)thiazol-2-amine

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

: 901309-40-8
tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

Guidance literature:: With dmap; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmcl.2013.05.025

Reference yield:

: 1480-87-1
2-fluoro-3-nitropyridine

: 901309-40-8
tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / N,N-dimethyl-formamide / 144 h / 130 °C

2: palladium 10% on activated carbon; hydrogen / methanol; tetrahydrofuran

3: dichloromethane / 2 h / 50 °C

4: lithium hydroxide / methanol; tetrahydrofuran / 2 h / 50 °C

5: 2,6-dimethylpyridine / ethanol / 90 °C

6: N-Bromosuccinimide; acetic acid / tetrahydrofuran / 20 °C

7: dmap / tetrahydrofuran / 20 °C

With 2,6-dimethylpyridine; dmap; N-Bromosuccinimide; palladium 10% on activated carbon; hydrogen; potassium carbonate; acetic acid; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2013.05.025

Reference yield:

: 901309-17-9
1-(2-[2-(tert-butyl)phenoxy]pyridin-3-yl)thiourea

: 901309-40-8
tert-Butyl 5-bromo-4-(trifluoromethyl)thiazol-2-yl(2-(2-tert-butylphenoxy)pyridin-3-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 2,6-dimethylpyridine / ethanol / 90 °C

2: N-Bromosuccinimide; acetic acid / tetrahydrofuran / 20 °C

3: dmap / tetrahydrofuran / 20 °C

With 2,6-dimethylpyridine; dmap; N-Bromosuccinimide; acetic acid; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmcl.2013.05.025