N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

Base Information

Chemical Name:N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide
CAS No.:1382723-29-6
Molecular Formula:C₂₁H₂₆N₂O₃
Molecular Weight:354.449
Hs Code.:

Synonyms:N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

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Chemical Property of N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

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Technology Process of N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

There total 1 articles about N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)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:

: 52085-14-0
4-benzoxy-salicylaldehyde

: 1382723-29-6
N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 0 °C

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / N,N-dimethyl-formamide / 16 h / Inert atmosphere; Sealed tube; Reflux

3: ammonium acetate / 50 °C

4: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 - 20 °C / Inert atmosphere

5: triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere

6: palladium 10% on activated carbon; hydrogen / methanol / 12 h

With lithium aluminium tetrahydride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; ammonium acetate; hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 2: Suzuki coupling / 3: Henry reaction;
DOI:10.1021/jm300544c

Reference yield:

: 1382723-29-6
N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

: 301187-46-2
(3aR,4S,7R,7aR)-7-methoxy-6,6-dimethyl-2-oxo-tetrahydro-3aH-[1,3]-dioxolo[4,5-c]pyran-4-yl 2,2,2-trichloroacetimidate

: C₃₀H₃₈N₂O₈

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/jm300544c

Reference yield:

: 1382723-29-6
N-(2-(5-hydroxy-3'-(morpholinomethyl)[1,1'-biphenyl]-2-yl)ethyl)acetamide

: 301187-46-2
(3aR,4S,7R,7aR)-7-methoxy-6,6-dimethyl-2-oxo-tetrahydro-3aH-[1,3]-dioxolo[4,5-c]pyran-4-yl 2,2,2-trichloroacetimidate

: 1382723-45-6
N-[2-(5-{[(3R,4S,5R)-3,4-dihydroxy-5-methoxy-6,6-dimethyltetrahydro-2H-pyran-2-yl]oxy}-3'-(morpholinomethyl)-[1,1'-biphenyl]-2-yl)ethyl]acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: boron trifluoride diethyl etherate / dichloromethane / 2 h / 20 °C

2: triethylamine / methanol / 12 h / 20 °C

With boron trifluoride diethyl etherate; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jm300544c