1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

Base Information

Chemical Name:1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone
CAS No.:1089729-26-9
Molecular Formula:C₂₂H₂₁ClN₂O₂S
Molecular Weight:412.94
Hs Code.:

Synonyms:1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

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Chemical Property of 1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

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Technology Process of 1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

There total 5 articles about 1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone 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: 46.0%

: 1089729-80-5
(R)-2-[4-(4-chloro-phenyl)-thiazol-2-yl]-piperidinium trifluoroacetate

: 701-99-5
Phenoxyacetyl chloride

: 1089729-26-9
1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

Guidance literature:: With triethylamine; dmap; In dichloromethane; at 20 ℃; for 16h;

Reference yield:

: 1089729-73-6
(R)-2-[4-(4-chloro-phenyl)-thiazol-2-yl]-piperidine-1-carboxylic acid tert-butyl ester

: 1089729-26-9
1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 0.5 h / 20 °C

2: triethylamine / dmap / dichloromethane / 16 h / 20 °C

With triethylamine; dmap; In dichloromethane;

Reference yield:

: 848488-91-5
tert-butyl (R)-2-carbamoylpiperidine-1-carboxyl-ate

: 1089729-26-9
1-{(R)-2-[4-(4-Chloro-phenyl)-thiazol-2-yl]-piperidin-1-yl}-2-phenoxy-ethanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: Lawessons reagent / 1,4-dioxane / 20 °C

2.1: sodium hydrogencarbonate / 1,2-dimethoxyethane / 24 h / 20 °C

2.2: 0.5 h / 0 - 20 °C

3.1: dichloromethane / 0.5 h / 20 °C

4.1: triethylamine / dmap / dichloromethane / 16 h / 20 °C

With Lawessons reagent; sodium hydrogencarbonate; triethylamine; dmap; In 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane;