4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

Base Information

Chemical Name:4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine
CAS No.:1430334-20-5
Molecular Formula:C₁₆H₁₈N₆O₃
Molecular Weight:342.357
Hs Code.:

Synonyms:4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

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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 4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

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Technology Process of 4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

There total 2 articles about 4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine 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: 94.0%

: 1430334-15-8
4-(4-(2-nitrobenzyl)imidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

: 1430334-20-5
4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

Guidance literature:: With platinum(IV) oxide; hydrogen; In methanol; for 20h; Inert atmosphere;
DOI:10.1016/j.tet.2013.03.039

Reference yield:

: 3160-91-6,7420-18-0
moroxydine hydrochloride

: 1430334-20-5
4-(4-(2-nitrobenzyl)-3,4-dihydroimidazo[1,2-a][1,3,5]triazin-2-yl)morpholine

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 0.33 h / 70 °C / Microwave irradiation

2: dimethyl sulfoxide; water / 7 h / 120 °C

3: platinum(IV) oxide; hydrogen / methanol / 20 h / Inert atmosphere

With platinum(IV) oxide; hydrogen; In tetrahydrofuran; methanol; water; dimethyl sulfoxide;
DOI:10.1016/j.tet.2013.03.039