N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

Base Information

Chemical Name:N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester
CAS No.:1349193-20-9
Molecular Formula:C₂₁H₂₂N₄O₆
Molecular Weight:426.429
Hs Code.:

N-[N<sub>4</sub>-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

Synonyms:N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

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Chemical Property of N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

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Technology Process of N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

There total 2 articles about N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester 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: 51.0%

: 1349193-19-6
N-(propyn-3-yl)glycine ethyl ester trifluoroacetate

: 144564-95-4
[N⁴-[(benzyloxy)carbonyl]cytosine-1-yl]acetic acid

: 1349193-20-9
N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

Guidance literature:: [N⁴-[(benzyloxy)carbonyl]cytosine-1-yl]acetic acid; With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

N-(propyn-3-yl)glycine ethyl ester trifluoroacetate; With triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.tet.2011.09.124

Reference yield:

: 1349193-15-2
N-(tert-butoxycarbonyl)-N-(propyn-3-yl)glycine ethyl ester

: 1349193-20-9
N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloromethane / 1 h / 20 °C

2.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 0.25 h / 20 °C

2.2: 20 °C

With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2011.09.124

Reference yield: 76.0%

: 950683-55-3
{2-[2-(2-azidoethoxy)ethoxy]ethyl}carbamic acid tert-butyl ester

: 1349193-20-9
N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]-N-(propyn-3-yl)glycine ethyl ester

: 1349193-23-2
N-[N₁-(8-tert-butoxycarbonylamino-3,6-dioxaoct-1-yl)-1,2,3-triazol-4-yl]methyl-N-[N₄-(benzyloxycarbonyl)cytosin-1-ylacetyl]glycine ethyl ester

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In dichloromethane; water; tert-butyl alcohol; at 20 ℃; for 48h;
DOI:10.1016/j.tet.2011.09.124