5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

Base Information

Chemical Name:5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione
CAS No.:188427-78-3
Molecular Formula:C₃₆H₃₆N₆O₆
Molecular Weight:648.718
Hs Code.:

5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

Synonyms:5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

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Chemical Property of 5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

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Technology Process of 5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

There total 7 articles about 5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione 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:

: 146443-42-7
1,3,4,6-Tetrakis(chloromethyl)tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione

: 188427-78-3
5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

Guidance literature:: Multi-step reaction with 7 steps

1: SnCl₄ / 1,2-dichloro-ethane / -35 - 0 °C

2: 65 percent / p-TsOH*H₂O / Heating

3: 88 percent / SnCl₄ / 1,2-dichloro-ethane / -35 - 0 °C

4: 80 percent / 53percent HNO₃ / acetic anhydride / 16 h / Ambient temperature

5: 94 percent / 53percent HNO₃ / acetic anhydride / 16 h / Ambient temperature

6: 96 percent / acetic anhydride; trifluoroacetic acid / 1 h / 95 °C

7: triethylammonium formate / Pd on carbon / methanol; tetrahydrofuran / 16 h

With nitric acid; tin(IV) chloride; triethylammonium formate; toluene-4-sulfonic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; acetic anhydride; 1,2-dichloro-ethane; trifluoroacetic acid;
DOI:10.1021/jo961382n

Reference yield:

: 150-78-7
1,4-dimethoxybezene

: 188427-78-3
5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

Guidance literature:: Multi-step reaction with 5 steps

1: 58 percent / SnCl₄ / 1,2-dichloro-ethane / -35 - 0 °C

2: 80 percent / 53percent HNO₃ / acetic anhydride / 16 h / Ambient temperature

3: 94 percent / 53percent HNO₃ / acetic anhydride / 16 h / Ambient temperature

4: 96 percent / acetic anhydride; trifluoroacetic acid / 1 h / 95 °C

5: triethylammonium formate / Pd on carbon / methanol; tetrahydrofuran / 16 h

With nitric acid; tin(IV) chloride; triethylammonium formate; palladium on activated charcoal; In tetrahydrofuran; methanol; acetic anhydride; 1,2-dichloro-ethane; trifluoroacetic acid;
DOI:10.1021/jo961382n

Reference yield:

: 188427-77-2
5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-dinitro-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

: 188427-78-3
5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetramethoxy-2,3-diamino-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno(2,1,8-ija)benz[f]azulene-6,13-dione

Guidance literature:: With triethylammonium formate; palladium on activated charcoal; In tetrahydrofuran; methanol; for 16h;
DOI:10.1021/jo961382n