(O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

Base Information

Chemical Name:(O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester
CAS No.:1346693-96-6
Molecular Formula:C₄₀H₄₁N₅O₁₀
Molecular Weight:751.793
Hs Code.:

Synonyms:(O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

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Chemical Property of (O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

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Technology Process of (O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

There total 3 articles about (O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl 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: 33.0%

: 1346434-13-6
O-(9-fluorenylmethyl)-N-phenyl-N-chloromethyl carbamate

: 1346434-12-5
N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

: 1346693-96-6
(O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

Guidance literature:: With triethylamine; In dichloromethane; for 2h; Reflux;

Reference yield:

: 143966-57-8
(S)-allyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate

: 1346693-96-6
(O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / 1,4-dioxane / 0.67 h / 20 °C

2: triethylamine / tetrahydrofuran / 0.5 h / 20 °C

3: triethylamine / dichloromethane / 2 h / Reflux

With hydrogenchloride; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;

Reference yield:

: N-(tert-butoxycarbonyl)-L-serine allyl ester hydrochloride

: 1346693-96-6
(O-(N-((9-fluorenylmethoxy)carbonyl)-N-phenyl)aminomethyl)-N-(6-(2,4-dinitrophenyl)amino)hexanoyl-L-serine allyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0.5 h / 20 °C

2: triethylamine / dichloromethane / 2 h / Reflux

With triethylamine; In tetrahydrofuran; dichloromethane;