2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

Base Information

Chemical Name:2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one
CAS No.:190334-09-9
Molecular Formula:C₁₈H₁₁N₅OS
Molecular Weight:345.384
Hs Code.:

Synonyms:2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

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Chemical Property of 2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

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Technology Process of 2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

There total 3 articles about 2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-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: 55.0%

: 103-72-0
phenyl isothiocyanate

: 190334-07-7
3-Amino-1H-pyrrolo[2,3-b]quinoxaline-2-carboxylic acid ethyl ester

: 190334-09-9
2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

Guidance literature:: In pyridine; for 8h; Heating;
DOI:10.1007/BF00807794

Reference yield:

: 40254-89-5
3-chloro-2-quinoxalinecarbonitrile

: 190334-09-9
2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / K₂CO₃ / dimethylformamide / 8 h / 70 °C

2: 74 percent / NaOEt / ethanol / 0.5 h / Heating

3: 55 percent / pyridine / 8 h / Heating

With sodium ethanolate; potassium carbonate; In pyridine; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 160315-00-4
ethyl 2-acetate

: 190334-09-9
2-Phenyl-3-thioxo-2,3,4,11-tetrahydro-2,4,5,10,11-pentaaza-benzo[b]fluoren-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / NaOEt / ethanol / 0.5 h / Heating

2: 55 percent / pyridine / 8 h / Heating

With sodium ethanolate; In pyridine; ethanol;