(Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

Base Information

Chemical Name:(Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate
CAS No.:1450915-10-2
Molecular Formula:C₃₈H₂₆BrN₃O₃S
Molecular Weight:684.613
Hs Code.:

Synonyms:(Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

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Chemical Property of (Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

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Technology Process of (Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

There total 4 articles about (Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate 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:

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 1450915-10-2
(Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

Guidance literature:: Multi-step reaction with 4 steps

1: bromine; acetic acid / 1 h / 0 - 5 °C

2: hydrazine hydrate / 6 h / 140 °C

3: piperidine / ethanol / 6 h / Reflux

4: copper peroxide / 20 h / Inert atmosphere; Sealed tube; Heating

With piperidine; copper peroxide; bromine; hydrazine hydrate; acetic acid; In ethanol; 2: |Wolff-Kishner Reduction / 3: |Knoevenagel Condensation / 4: |Ullmann Condensation;
DOI:10.1021/ol401527a

Reference yield:

: 20870-78-4
5-bromo-2-indolin-2-one

: 1450915-10-2
(Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine / ethanol / 6 h / Reflux

2: copper peroxide / 20 h / Inert atmosphere; Sealed tube; Heating

With piperidine; copper peroxide; In ethanol; 1: |Knoevenagel Condensation / 2: |Ullmann Condensation;
DOI:10.1021/ol401527a

Reference yield:

: 87-48-9
5-Bromo-1H-indole-2,3-dione

: 1450915-10-2
(Z)-methyl 6-(5-bromo-3-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)-2-oxoindolin-1-yl)nicotinate

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / 6 h / 140 °C

2: piperidine / ethanol / 6 h / Reflux

3: copper peroxide / 20 h / Inert atmosphere; Sealed tube; Heating

With piperidine; copper peroxide; hydrazine hydrate; In ethanol; 1: |Wolff-Kishner Reduction / 2: |Knoevenagel Condensation / 3: |Ullmann Condensation;
DOI:10.1021/ol401527a