(3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

Base Information

Chemical Name:(3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride
CAS No.:1379513-81-1
Molecular Formula:C₂₉H₃₁N₂O₅S*Cl
Molecular Weight:555.095
Hs Code.:

Synonyms:(3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

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Chemical Property of (3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

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Technology Process of (3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

There total 11 articles about (3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride 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: 74.0%

: 1379513-80-0
(R)-quinuclidin-3-yl 2-phenyl-2-(phenylsulfonamido)acetate

: 532-27-4,108321-66-0,164322-25-2
1-chloroacetophenone

: 1379513-81-1
(3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

Guidance literature:: In ethyl acetate; acetonitrile; at 20 ℃;

Reference yield:

: 2900-27-8,3601-66-9,14675-97-9,33125-05-2
2-(tert-butoxycarbonylamino)-2-phenylacetic acid

: 1379513-81-1
(3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

Guidance literature:: Multi-step reaction with 4 steps

1: dicyclohexyl-carbodiimide; benzotriazol-1-ol / tetrahydrofuran / 20 °C

2: hydrogenchloride / water; tetrahydrofuran / 15 h / 20 °C

3: triethylamine / dichloromethane / 4 h / 20 °C

4: ethyl acetate; acetonitrile / 20 °C

With hydrogenchloride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetonitrile;

Reference yield:

: 2835-06-5
phenylglycin

: 1379513-81-1
(3R)-1-(2-oxo-2-phenylethyl)-3-(2-phenyl-2-(phenylsulfonamido)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / water; acetone / 1 h / 20 °C

1.2: pH 5

2.1: dicyclohexyl-carbodiimide; benzotriazol-1-ol / tetrahydrofuran / 20 °C

3.1: hydrogenchloride / water; tetrahydrofuran / 15 h / 20 °C

4.1: triethylamine / dichloromethane / 4 h / 20 °C

5.1: ethyl acetate; acetonitrile / 20 °C

With hydrogenchloride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone; acetonitrile;