2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

Base Information

Chemical Name:2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide
CAS No.:911494-26-3
Molecular Formula:C₂₃H₂₄ClFN₄O₄
Molecular Weight:474.919
Hs Code.:

Synonyms:2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

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Chemical Property of 2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

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Technology Process of 2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

There total 6 articles about 2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-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:

: C₂₃H₂₂ClFN₄O₄

: 911494-26-3
2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

Guidance literature:: With sodium cyanoborohydride; acetic acid; In methanol;
DOI:10.1016/j.tetlet.2008.10.119

Reference yield:

: 911494-24-1
methyl 5-(benzoyloxy)-2-{2-(benzyloxy)-1-[(tert-butoxycarbonyl)amino]ethyl}-6-hydroxypyrimidine-4-carboxylate

: 911494-26-3
2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: methanol / 24 h / Heating / reflux

2: dichloromethane / 1.5 h / 20 °C

3: triethylamine; trimethyl orthoformate / 2 h / 20 °C

4: sodium cyanoborohydride; acetic acid / methanol / 20 °C / pH 5

With sodium cyanoborohydride; acetic acid; triethylamine; trimethyl orthoformate; In methanol; dichloromethane;

Reference yield:

: 911639-71-9
tert-butyl [(2E)-2-amino-1-[(benzyloxy)methyl]-2-(hydroxyimino)ethyl]carbamate

: 911494-26-3
2-{2-(benzyloxy)-1-[(2-chloroethyl)amino]ethyl}-N-(4-fluorobenzyl)-5,6-dihydroxypyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: chloroform; xylene / 26.5 h / 145 °C / Heating / reflux

1.2: 20 °C

2.1: methanol / 24 h / Heating / reflux

3.1: dichloromethane / 1.5 h / 20 °C

4.1: triethylamine; trimethyl orthoformate / 2 h / 20 °C

5.1: sodium cyanoborohydride; acetic acid / methanol / 20 °C / pH 5

With sodium cyanoborohydride; acetic acid; triethylamine; trimethyl orthoformate; In methanol; dichloromethane; chloroform; xylene;