1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

Base Information

Chemical Name:1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate
CAS No.:1416175-52-4
Molecular Formula:C₂₃H₃₂FNO₅S
Molecular Weight:453.575
Hs Code.:

Synonyms:1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

Suppliers and Price of 1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-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 1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

There total 8 articles about 1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-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:

: 1046817-22-4
1-methylcyclopropyl (4-nitrophenyl)carbonate

: 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane hydrochloride

: 1416175-52-4
1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

Guidance literature:: With triethylamine; In chloroform; at 20 ℃;
DOI:10.1016/j.bmc.2018.02.032

Reference yield:

: 203661-69-2
tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate

: 1416175-52-4
1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium tert-butylate / toluene / 0.33 h / 20 °C / Inert atmosphere

1.2: 4 h / 70 °C / Inert atmosphere

2.1: trifluoroacetic acid / acetonitrile; water / 1 h / 20 °C

3.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide; mineral oil / 0.33 h / Cooling with ice

3.2: 3 h / 20 °C

4.1: hydrogen; 20% palladium hydroxide-activated charcoal / ethanol / 20 °C

5.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 1 h / 0 °C

6.1: diamide; tributylphosphine / tetrahydrofuran / 60 °C

7.1: hydrogenchloride / ethyl acetate / 20 °C

8.1: triethylamine / chloroform / 20 °C

With hydrogenchloride; tributylphosphine; diamide; 20% palladium hydroxide-activated charcoal; potassium tert-butylate; hydrogen; sodium hydride; diisobutylaluminium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; chloroform; water; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile; mineral oil; 1.1: |Wittig Olefination / 1.2: |Wittig Olefination / 3.1: |Horner-Wadsworth-Emmons Olefination / 3.2: |Horner-Wadsworth-Emmons Olefination / 6.1: |Mitsunobu Displacement;
DOI:10.1016/j.bmc.2018.02.032

Reference yield:

: tert-butyl 2-(methoxymethylidene)-7-azaspiro[3.5]nonane-7-carboxylate

: 1416175-52-4
1-methylcyclopropyl 2-{3-[3-fluoro-4-(methanesulfonyl)phenoxy]propyl}-7-azaspiro[3.5]nonane-7-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: trifluoroacetic acid / acetonitrile; water / 1 h / 20 °C

2.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide; mineral oil / 0.33 h / Cooling with ice

2.2: 3 h / 20 °C

3.1: hydrogen; 20% palladium hydroxide-activated charcoal / ethanol / 20 °C

4.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 1 h / 0 °C

5.1: diamide; tributylphosphine / tetrahydrofuran / 60 °C

6.1: hydrogenchloride / ethyl acetate / 20 °C

7.1: triethylamine / chloroform / 20 °C

With hydrogenchloride; tributylphosphine; diamide; 20% palladium hydroxide-activated charcoal; hydrogen; sodium hydride; diisobutylaluminium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; chloroform; water; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile; mineral oil; 2.1: |Horner-Wadsworth-Emmons Olefination / 2.2: |Horner-Wadsworth-Emmons Olefination / 5.1: |Mitsunobu Displacement;
DOI:10.1016/j.bmc.2018.02.032