tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

Base Information

Chemical Name:tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate
CAS No.:1257387-96-4
Molecular Formula:C₂₄H₃₂F₂N₂O₄
Molecular Weight:450.526
Hs Code.:

Synonyms:tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

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Chemical Property of tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

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Technology Process of tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

There total 4 articles about tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-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: 29.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 1257387-95-3
(3R)-(3,5-difluorophenyl)-12-oxa-1,4-diazadispiro[5.2.5.2]hexadecan-5-one

: 1257387-96-4
tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 60 ℃;

Reference yield:

: 50675-18-8
3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde

: 1257387-96-4
tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / toluene / 6 h / Reflux

2.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 72 h / 50 °C / 2250.23 Torr / Inert atmosphere

3.1: N-benzyl-N,N,N-triethylammonium chloride; water; sodium hydroxide / dichloromethane / Cooling with acetone-dry ice

3.2: 0 - 20 °C

3.3: 0 °C / pH 1

4.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 60 °C

With sulfuric acid; N-benzyl-N,N,N-triethylammonium chloride; water; hydrogen; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium 10% on activated carbon; In dichloromethane; ethyl acetate; toluene; acetonitrile;

Reference yield:

: 1159280-52-0
9-oxaspiro[5.5]undec-4-en-3-one

: 1257387-96-4
tert-butyl (3R)-(3,5-difluorophenyl)-5-oxo-12-oxa-1,4-diaza-dispiro[5.2.5.2]hexadecane-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 72 h / 50 °C / 2250.23 Torr / Inert atmosphere

2.1: N-benzyl-N,N,N-triethylammonium chloride; water; sodium hydroxide / dichloromethane / Cooling with acetone-dry ice

2.2: 0 - 20 °C

2.3: 0 °C / pH 1

3.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 60 °C

With N-benzyl-N,N,N-triethylammonium chloride; water; hydrogen; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium 10% on activated carbon; In dichloromethane; ethyl acetate; acetonitrile;