(3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

Base Information

Chemical Name:(3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one
CAS No.:1447710-41-9
Molecular Formula:C₁₈H₁₃ClN₂O
Molecular Weight:308.767
Hs Code.:

Synonyms:(3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

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Chemical Property of (3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

Chemical Property:

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Technology Process of (3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

There total 3 articles about (3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one 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:

: 530-53-0
deoxyvasicinone

: 104-88-1
4-chlorobenzaldehyde

: 1447710-41-9
(3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; Reflux;
DOI:10.2174/1570180811310060008

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 1447710-41-9
(3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / benzene / Heating

2: benzene / 12 h / Cooling

3: potassium tert-butylate / tetrahydrofuran / Reflux

With thionyl chloride; potassium tert-butylate; In tetrahydrofuran; benzene;
DOI:10.2174/1570180811310060008

Reference yield:

: 60941-84-6
Sulfinamide Anhydride of Anthranilic Acid

: 1447710-41-9
(3E)-3-(4-chlorobenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / 12 h / Cooling

2: potassium tert-butylate / tetrahydrofuran / Reflux

With potassium tert-butylate; In tetrahydrofuran; benzene;
DOI:10.2174/1570180811310060008