5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

Base Information

Chemical Name:5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil
CAS No.:114894-46-1
Molecular Formula:C₃₀H₂₇N₃O₇
Molecular Weight:541.56
Hs Code.:

Synonyms:5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

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Chemical Property of 5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

Chemical Property:

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Technology Process of 5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

There total 6 articles about 5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil 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: 67.0%

: 114894-45-0
5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>-2-oxo-4-methoxypyrimidine

: 114894-46-1
5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

Guidance literature:: With hydrogenchloride; In ethanol; 1.) 50 deg C, 4 h; 2.) room temperature, overnight;
DOI:10.1002/jhet.5570240418

Reference yield:

: 90503-17-6
1-benzyloxy-2-chloromethoxy-3-phthaloylimidopropane

: 114894-46-1
5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

Guidance literature:: Multi-step reaction with 4 steps

1: 68 percent / Na₂CO₃ / CH₂Cl₂ / Ambient temperature

2: 83 percent / H₂, 6 N HCl / 5percent Pd on charcoal / CH₂Cl₂; methanol / 2280 Torr

3: 1.) sodium methoxide / 1.) methanol, 15 min; 2.) overnight, room temperature

4: 67 percent / conc. HCl / aq. ethanol / 1.) 50 deg C, 4 h; 2.) room temperature, overnight

With hydrogenchloride; hydrogen; sodium methylate; sodium carbonate; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
DOI:10.1002/jhet.5570240418

Reference yield:

: 1074-82-4
potassium phtalimide

: 114894-46-1
5-(3-benzyloxybenzyl)-1-<(1'-phthalimidomethyl-2'-hydroxyethoxy)methyl>uracil

Guidance literature:: Multi-step reaction with 7 steps

2: BF₃

3: HCl(g)

4: 68 percent / Na₂CO₃ / CH₂Cl₂ / Ambient temperature

5: 83 percent / H₂, 6 N HCl / 5percent Pd on charcoal / CH₂Cl₂; methanol / 2280 Torr

6: 1.) sodium methoxide / 1.) methanol, 15 min; 2.) overnight, room temperature

7: 67 percent / conc. HCl / aq. ethanol / 1.) 50 deg C, 4 h; 2.) room temperature, overnight

With hydrogenchloride; boron trifluoride; hydrogen; sodium methylate; sodium carbonate; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
DOI:10.1002/jhet.5570240418