2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

Base Information

Chemical Name:2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide
CAS No.:1428548-50-8
Molecular Formula:C₂₁H₁₉N₃O₆
Molecular Weight:409.398
Hs Code.:

Synonyms:2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

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Chemical Property of 2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

Chemical Property:

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Technology Process of 2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

There total 5 articles about 2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide 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:

: 1428548-49-5
N-[bis(4-methoxyphenyl)methyl]-2-formyl-4-hydroxypyrimidine-5-carboxamide

: 1428548-50-8
2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

Guidance literature:: With sodium chlorite; sodium hydrogenphosphate dodecahydrate; In tert-butyl alcohol; at 20 ℃; for 2h;

Reference yield:

: 1428548-40-6
ethyl 2-((benzyloxy)methyl)-4-hydroxypyrimidine-5-carboxylate

: 1428548-50-8
2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: water; potassium hydroxide / 1 h / 70 °C

2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide; N,N-dimethyl-formamide / 20 °C

3: palladium on activated charcoal; ammonium formate / methanol / Reflux

4: Dess-Martin periodane / dichloromethane / 1 h / 20 °C

5: sodium chlorite; sodium hydrogenphosphate dodecahydrate / tert-butyl alcohol / 2 h / 20 °C

With sodium chlorite; sodium hydrogenphosphate dodecahydrate; palladium on activated charcoal; water; ammonium formate; Dess-Martin periodane; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 1428548-41-7
2-((benzyloxy)methyl)-4-hydroxypyrimidine-5-carboxylic acid

: 1428548-50-8
2-[(benzyloxy)methyl]-N-[bis(4-methoxyphenyl)methyl]-4-hydroxypyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide; N,N-dimethyl-formamide / 20 °C

2: palladium on activated charcoal; ammonium formate / methanol / Reflux

3: Dess-Martin periodane / dichloromethane / 1 h / 20 °C

4: sodium chlorite; sodium hydrogenphosphate dodecahydrate / tert-butyl alcohol / 2 h / 20 °C

With sodium chlorite; sodium hydrogenphosphate dodecahydrate; palladium on activated charcoal; ammonium formate; Dess-Martin periodane; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol;