2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-one

Base Information

Chemical Name:2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-one
CAS No.:89374-50-5
Molecular Formula:C₁₉H₁₃N₃OS
Molecular Weight:331.398
Hs Code.:
DSSTox Substance ID:DTXSID30530244
Wikidata:Q82401253

Synonyms:89374-50-5;2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-one;DTXSID30530244

Suppliers and Price of 2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-one

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-one

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:331.07793322
Heavy Atom Count:24
Complexity:465

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N(C2=CC=CC=C2)C3=NC(=O)C4=C(S3)N=CC=C4

Technology Process of 2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-one

There total 2 articles about 2-(Diphenylamino)-4H-pyrido[3,2-e][1,3]thiazin-4-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: 35.0%

: 89374-20-9
2-Chloronicotinoyl Isothiocyanate

: 122-39-4
diphenylamine

: 89374-50-5
2-Diphenylamino-pyrido[3,2-e][1,3]thiazin-4-one

Guidance literature:: In acetone; 1)stirring 30 min 2)briefly boiled;
DOI:10.1135/cccc19833315

Reference yield:

: 49609-84-9
2-Chloronicotinoyl chloride

: 89374-50-5
2-Diphenylamino-pyrido[3,2-e][1,3]thiazin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 0.08 h / 40 °C

2: 35 percent / acetone / 1)stirring 30 min 2)briefly boiled

In acetone;
DOI:10.1135/cccc19833315