tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate
CAS No.:1403676-70-9
Molecular Formula:C₂₃H₃₅FN₂O₆S
Molecular Weight:486.605
Hs Code.:

Synonyms:tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Suppliers and Price of tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

There total 8 articles about tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-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:

: C₂₃H₃₅FN₂O₅S

: 1403676-70-9
tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Guidance literature:: C₂₃H₃₅FN₂O₅S; With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 1h;

With hydrogenchloride; In methanol; water; at 20 ℃; for 0.25h;

Reference yield:

: 1489-97-0
ethyl 1,4-dioxaspiro[4.5]decane-8-carboxylate

: 1403676-70-9
tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium borohydride / tetrahydrofuran / 20 h / Inert atmosphere; Reflux

1.2: 0.5 h / 0 - 20 °C

2.1: triethylamine / dichloromethane / 4.5 h / 0 - 20 °C / Inert atmosphere

3.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 100 °C / Inert atmosphere

4.1: hydrogenchloride / water; tetrahydrofuran / 42 h / 50 °C

5.1: toluene-4-sulfonic acid / toluene / 96 h / 150 °C

5.2: 3 h / 20 °C / Cooling with ice

5.3: 20 °C

6.1: sodium hydroxide; dihydrogen peroxide / tetrahydrofuran; methanol / 1 h / 20 °C

6.2: 0.25 h / 20 °C

With hydrogenchloride; lithium borohydride; dihydrogen peroxide; caesium carbonate; triethylamine; sodium hydroxide; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 23521-81-5,17159-82-9
(1,4-dioxaspiro[4.5]dec-8-yl)methanol

: 1403676-70-9
tert-butyl 4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-2-hydroxycyclohexyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / dichloromethane / 4.5 h / 0 - 20 °C / Inert atmosphere

2.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 100 °C / Inert atmosphere

3.1: hydrogenchloride / water; tetrahydrofuran / 42 h / 50 °C

4.1: toluene-4-sulfonic acid / toluene / 96 h / 150 °C

4.2: 3 h / 20 °C / Cooling with ice

4.3: 20 °C

5.1: sodium hydroxide; dihydrogen peroxide / tetrahydrofuran; methanol / 1 h / 20 °C

5.2: 0.25 h / 20 °C

With hydrogenchloride; dihydrogen peroxide; caesium carbonate; triethylamine; sodium hydroxide; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;