7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

Base Information

Chemical Name:7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester
CAS No.:860265-91-4
Molecular Formula:C₃₇H₃₇FN₂O₁₄
Molecular Weight:752.704
Hs Code.:

7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

Synonyms:7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

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Chemical Property of 7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

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Technology Process of 7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

There total 1 articles about 7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl 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: 46.9%

: 15014-25-2
malonic acid dibenzyl ester

: 299172-14-8
[(2-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-4-formyl-5-hydroxyphenyl)methoxycarbonylmethylamino]acetic acid methyl ester

: 860265-91-4
7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

Guidance literature:: With piperidine; In acetonitrile; benzene; for 24h; Heating;
DOI:10.1021/ja0528228

Reference yield: 56.2%

: 860265-91-4
7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

: 860265-92-5
7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid

Guidance literature:: With palladium on activated charcoal; cyclohexene; In ethanol; at 50 ℃; for 24h;
DOI:10.1021/ja0528228

Reference yield:

: 860265-91-4
7-bis(methoxycarbonylmethyl)amino-6-{2-[6-bis(methoxycarbonylmethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid benzyl ester

: 860265-93-6
7-bis(carboxymethyl)amino-6-{2-[6-bis(carboxymethyl)amino-3-fluorophenoxy]ethoxy}-2-oxo-2H-chromene-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 56.2 percent / Pd/C; cyclohexene / ethanol / 24 h / 50 °C

2: 45.5 percent / LiI / acetonitrile / 120 h / Heating

With palladium on activated charcoal; lithium iodide; cyclohexene; In ethanol; acetonitrile;
DOI:10.1021/ja0528228