{4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

Base Information

Chemical Name:{4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester
CAS No.:928038-10-2
Molecular Formula:C₃₃H₂₄FN₃O₇
Molecular Weight:593.568
Hs Code.:

Synonyms:{4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

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Chemical Property of {4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

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Technology Process of {4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

There total 3 articles about {4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl 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:

: 864245-96-5
[4-(2-aminopyridin-4-yloxy)-3-fluorophenyl]carbamic acid benzyl ester

: 1885-14-9
phenyl chloroformate

: 928038-10-2
{4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; for 0.5h;

Reference yield:

: 864245-94-3
4-(4-Benzyloxycarbonylamino-2-fluorophenoxy)pyridine-2-carboxylic acid

: 928038-10-2
{4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: diphenyl phosphoryl azide; triethylamine / 21.75 h / 20 - 90 °C

2.1: hydrogenchloride / ethyl acetate / 16 h / 0 - 20 °C

2.2: 0.5 h

3.1: triethylamine / tetrahydrofuran / 0.5 h / 0 - 20 °C

With hydrogenchloride; diphenyl phosphoryl azide; triethylamine; In tetrahydrofuran; ethyl acetate;

Reference yield:

: 864245-95-4
[4-(4-Benzyloxycarbonylamino-2-fluorophenoxy)pyridin-2-yl]carbamic acid tert-butyl ester

: 928038-10-2
{4-[4-(benzyloxycarbonylamino)-2-fluorophenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / ethyl acetate / 16 h / 0 - 20 °C

1.2: 0.5 h

2.1: triethylamine / tetrahydrofuran / 0.5 h / 0 - 20 °C

With hydrogenchloride; triethylamine; In tetrahydrofuran; ethyl acetate;