1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-[(4-methylphenyl)amino]-

Base Information

Chemical Name:1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-[(4-methylphenyl)amino]-
CAS No.:63351-31-5
Molecular Formula:C₁₄H₁₅N₅O₂
Molecular Weight:285.305
Hs Code.:

Synonyms:8-(4-Methylphenylamino)-theophyllin;8-(p-Tolylamino)theophyllin;1,3-Dimethyl-8-p-tolylamino-3,7-dihydro-purine-2,6-dione;

Suppliers and Price of 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-[(4-methylphenyl)amino]-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-[(4-methylphenyl)amino]-

Chemical Property:

PSA：84.71000
LogP:1.08530

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-[(4-methylphenyl)amino]-

There total 5 articles about 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-[(4-methylphenyl)amino]- 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: 78.0%

: 10381-75-6
8-bromotheophylline

: 106-49-0,12221-03-3
p-toluidine

: 63351-31-5
1,3-dimethyl-8-(4-methyl-anilino)-3,7⁽⁹⁾-dihydro-purine-2,6-dione

Guidance literature:: In various solvent(s); for 15h; Heating;
DOI:10.1002/jhet.5570310515

Reference yield:

: 6642-31-5
6-Amino-1,3-dimethylbarbituric acid

: 63351-31-5
1,3-dimethyl-8-(4-methyl-anilino)-3,7⁽⁹⁾-dihydro-purine-2,6-dione

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 6 h / Heating

2: 1.) trimethylsilyl azide / 1.) chloroform, a.) 0 deg C, 5 h, b.) RT, 13 h, 2.) chloroform, a.) RT, 5 h, b.) reflux, 2 h

3: 20percent aq. KHCO₃ / Heating

With trimethylsilylazide; potassium hydrogencarbonate; In chloroform;
DOI:10.1002/jhet.5570310515