tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate
CAS No.:1427659-87-7
Molecular Formula:C₂₅H₃₃N₃O₄S
Molecular Weight:471.621
Hs Code.:

Synonyms:tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

Chemical Property:

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Technology Process of tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

There total 1 articles about tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-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:

: 1313010-11-5
tert-butyl 4-{4-[(Z/E)-(hydroxyimino)methyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

: 1415385-81-7
4, 5-dimethyl-2-(prop-1-en-2-yl)phenol

: 1427659-87-7
tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

Guidance literature:: With N-chloro-succinimide; water; potassium hydrogencarbonate; In ethyl acetate; for 0.666667h; Reflux;

Reference yield:

: 1427659-87-7
tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

: 106-96-7
propargyl bromide

: 1427659-88-8
tert-butyl 4-(4-{5-[4,5-dimethyl-2-(prop-2-yn-1-yloxy)phenyl]-5-methyl-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In acetone; toluene; at 60 ℃; for 6h;

Reference yield:

: 1427659-87-7
tert-butyl 4-{4-[5-(2-hydroxy-4,5-dimethylphenyl)-5-methyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

: 1427659-65-1
2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[4,5-dimethyl-2-(prop-2-yn-1-yloxy)phenyl]-5-methyl-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / acetone; toluene / 6 h / 60 °C

2.1: hydrogenchloride / 1,4-dioxane / 20 °C

3.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 0 - 20 °C

3.2: 20 °C

With hydrogenchloride; oxalyl dichloride; potassium carbonate; N,N-dimethyl-formamide; In 1,4-dioxane; dichloromethane; acetone; toluene;