(2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

Base Information

Chemical Name:(2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol
CAS No.:1421850-04-5
Molecular Formula:C₁₈H₂₁N₃O₂S
Molecular Weight:343.45
Hs Code.:

Synonyms:(2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

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Chemical Property of (2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

Chemical Property:

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Technology Process of (2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

There total 6 articles about (2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol 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:

: 1421850-03-4
ethyl 2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazole-4-carboxylate

: 1421850-04-5
(2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h;

Reference yield:

: 2881-83-6
ethyl 4-methoxybenzoylacetate

: 1421850-04-5
(2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: toluene / 14 h / 90 °C

1.2: 20 h / 80 °C

2.1: sodium hydroxide; water / ethanol; tetrahydrofuran / 1 h / 20 °C

3.1: thionyl chloride / toluene / 2.5 h / 100 °C

3.2: 14 h / 20 °C

4.1: Lawessons reagent / tetrahydrofuran / 0.33 h / 60 °C

5.1: ethanol / 14 h / 90 °C

6.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C

With Lawessons reagent; lithium aluminium tetrahydride; thionyl chloride; water; sodium hydroxide; In tetrahydrofuran; ethanol; toluene;

Reference yield:

: 1245207-16-2
ethyl 1-tert-butyl-5-(4-methoxyphenyl)-1H-pyrazole-4-carboxylate

: 1421850-04-5
(2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-4-yl)methanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide; water / ethanol; tetrahydrofuran / 1 h / 20 °C

2.1: thionyl chloride / toluene / 2.5 h / 100 °C

2.2: 14 h / 20 °C

3.1: Lawessons reagent / tetrahydrofuran / 0.33 h / 60 °C

4.1: ethanol / 14 h / 90 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C

With Lawessons reagent; lithium aluminium tetrahydride; thionyl chloride; water; sodium hydroxide; In tetrahydrofuran; ethanol; toluene;