5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

Base Information

Chemical Name:5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride
CAS No.:76896-24-7
Molecular Formula:C₁₈H₁₈N₃*Cl
Molecular Weight:311.814
Hs Code.:

Synonyms:5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

Suppliers and Price of 5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

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Technology Process of 5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

There total 3 articles about 5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride 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:

: 67397-05-1
1-(2-hydroxyethyl)-5-phenyl-1,2,3,5-tetrahydroimidazo<2,1-b>quinazoline

: 76896-24-7
5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / thionyl chloride / CHCl₃ / 2 h / Ambient temperature

2: ethanol / 3 h / Heating

With thionyl chloride; In ethanol; chloroform;
DOI:10.1248/cpb.28.2587

Reference yield:

: 70888-29-8
2-chloro-3-(2-chloroethyl)-4-phenyl-3,4-dihydroquinazoline

: 76896-24-7
5-phenyl-1,2,3,5-tetrahydro-5H-2a,4a,9b-triazapentaleno<1.6-a,b>naphthalenium chloride

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / ethanol / 5 h / Heating

2: 93 percent / thionyl chloride / CHCl₃ / 2 h / Ambient temperature

3: ethanol / 3 h / Heating

With thionyl chloride; In ethanol; chloroform;
DOI:10.1248/cpb.28.2587