(3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

Base Information

Chemical Name:(3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione
CAS No.:109519-86-0
Molecular Formula:C₃₅H₃₁N₅O₄S
Molecular Weight:617.728
Hs Code.:

Synonyms:(3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

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Chemical Property of (3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

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Technology Process of (3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

There total 5 articles about (3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-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: 66.0%

: 109519-77-9
C₃₅H₃₃N₅O₄S

: 109519-86-0
(3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

Guidance literature:: With lead(IV) acetate; In acetonitrile; at -5 ℃;
DOI:10.1248/cpb.34.3994

Reference yield:

: 107733-62-0
benzyl crotyl amine

: 109519-86-0
(3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 32 percent / ethanol / 12 h / Heating

2: 78 percent / conc. hydrochloric acid / methanol / 0 °C

3: 66 percent / lead tetraacetate / acetonitrile / -5 °C

With lead(IV) acetate; hydrogenchloride; In methanol; ethanol; acetonitrile;
DOI:10.1248/cpb.34.3994

Reference yield:

: 109519-69-9
6-[Benzyl-((E)-but-2-enyl)-amino]-2,4-dioxo-1,3-diphenyl-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde

: 109519-86-0
(3S,3aS)-5-Benzyl-3-methyl-6,8-diphenyl-2-(toluene-4-sulfonyl)-2,3,3a,4,5,6-hexahydro-1,2,5,6,8-pentaaza-cyclopenta[a]naphthalene-7,9-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / conc. hydrochloric acid / methanol / 0 °C

2: 66 percent / lead tetraacetate / acetonitrile / -5 °C

With lead(IV) acetate; hydrogenchloride; In methanol; acetonitrile;
DOI:10.1248/cpb.34.3994