5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

Base Information

Chemical Name:5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine
CAS No.:130699-89-7
Molecular Formula:C₅₀H₅₄N₆O₉
Molecular Weight:883.014
Hs Code.:

5'-O-<bis(4-methoxyphenyl)phenylmethyl>-5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

Synonyms:5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

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Chemical Property of 5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

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Technology Process of 5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

There total 2 articles about 5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine 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: 48.0%

: 96203-41-7
5'-O-DMT-5-<3-<(2-aminoethyl)-amino>-3-oxopropyl>-2'-deoxyuridine

: 130699-87-5
4-<3-carbonyl-3-(p-nitrophenoxy)propyl>-4'-methyl-2,2'-bipyridine

: 130699-89-7
5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

Guidance literature:: With triethylamine; In acetonitrile; for 24h; Ambient temperature;
DOI:10.1021/ja00001a041

Reference yield:

: 114527-28-5
4-(4′-methyl-[2,2′-bipyridin]-4-yl)butanoic acid

: 130699-89-7
5'-O--5-<3-<<2-<<4-(4'-methyl-2,2'-bipyridin-4-yl)-1-oxobutyl>amino>ethyl>amino>-3-oxopropyl>-2'-deoxyuridine

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / DCC / CH₂Cl₂ / 12 h / Ambient temperature

2: 48 percent / Et₃N / acetonitrile / 24 h / Ambient temperature

With triethylamine; dicyclohexyl-carbodiimide; In dichloromethane; acetonitrile;
DOI:10.1021/ja00001a041