(3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

Base Information

Chemical Name:(3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate
CAS No.:1616455-80-1
Molecular Formula:C₃₁H₂₉N₃O₅
Molecular Weight:523.588
Hs Code.:

Synonyms:(3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

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Chemical Property of (3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

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Technology Process of (3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

There total 9 articles about (3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate 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: 49.0%

: 1616455-78-7
3-allyl-2-oxo-2,3-dihydro-1,3-benzoxazole-6-carbaldehyde

: 1616455-79-8
(3R)-1-azabicyclo[2.2.2]oct-3-yl (4-bromobiphenyl-2-yl)carbamate

: 1616455-80-1
(3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

Guidance literature:: With palladium diacetate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In acetonitrile; at 90 ℃; for 6h; Sealed tube; Inert atmosphere;

Reference yield:

: 1616455-77-6
3-allyl-2-oxo-2,3-dihydro-1,3-benzoxazole-6-carbonitrile

: 1616455-80-1
(3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: formic acid / 75 °C

2: tris-(o-tolyl)phosphine; N-ethyl-N,N-diisopropylamine; palladium diacetate / acetonitrile / 6 h / 90 °C / Sealed tube; Inert atmosphere

With formic acid; palladium diacetate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In acetonitrile; 2: |Heck Reaction;

Reference yield:

: 64085-52-5
5-bromo-2-iodo-aniline

: 1616455-80-1
(3R)-1-azabicyclo[2.2.2]oct-3-yl {4-[(1E)-3-(6-formyl-2-oxo-1,3-benzoxazol-3(2H)-yl)prop-1-en-1-yl]biphenyl-2-yl}carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / 1,4-dioxane / 3 h / 110 °C / Inert atmosphere

2: triethylamine / toluene / 2 h / 0 - 20 °C

3: toluene / 2 h / 120 °C

4: tris-(o-tolyl)phosphine; N-ethyl-N,N-diisopropylamine; palladium diacetate / acetonitrile / 6 h / 90 °C / Sealed tube; Inert atmosphere

With palladium diacetate; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In 1,4-dioxane; toluene; acetonitrile; 4: |Heck Reaction;