(E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

Base Information

Chemical Name:(E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide
CAS No.:868407-38-9
Molecular Formula:C₂₅H₂₆Cl₂FN₃O₂
Molecular Weight:490.405
Hs Code.:

Synonyms:(E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

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Chemical Property of (E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

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Technology Process of (E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

There total 5 articles about (E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide 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: 81.0%

: (E)-3-(2-amino-4-chlorophenyl)-1-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-propenone

: 79-04-9
chloroacetyl chloride

: 868407-38-9
(E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 685534-21-8
(E)-3-(2-tert-butoxycarbonylamino-4-chlorophenyl)-acrylic acid methyl ester

: 868407-38-9
(E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: methanol; sodium hydroxide; water / 1 h / 50 °C

1.2: pH 3 / Acidic aqueous solution

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h

3.1: hydrogenchloride; ethanol; water / 1 h / 20 °C

4.1: triethylamine / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; methanol; sodium hydroxide; ethanol; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 685534-22-9
(E)-3-(2-tert-butoxycarbonylamino-4-chlorophenyl)-acrylic acid

: 868407-38-9
(E)-2-chloro-N-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,9-diazabicyclo[3.3.1]non-9-yl]-3-oxopropenyl}-phenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h

2: hydrogenchloride; ethanol; water / 1 h / 20 °C

3: triethylamine / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; ethanol; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane;