tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

Base Information

Chemical Name:tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate
CAS No.:1195781-45-3
Molecular Formula:C₁₇H₁₇FN₄O₃S
Molecular Weight:376.411
Hs Code.:

Synonyms:tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

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Chemical Property of tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

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Technology Process of tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

There total 4 articles about tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate 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: 35.0%

: 1195781-43-1
tert-butyl {3-fluoro-4-[(5-aminopyridin-2-yl)oxy]phenyl}carbamate

: 333-20-0
potassium thioacyanate

: 144-55-8
sodium hydrogencarbonate

: 1195781-45-3
tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

Guidance literature:: tert-butyl {3-fluoro-4-[(5-aminopyridin-2-yl)oxy]phenyl}carbamate; potassium thioacyanate; With bromine; In acetic acid; at 0 - 20 ℃;

sodium hydrogencarbonate; In water;

Reference yield:

: 859537-27-2
N-(3-fluoro-4-hydroxyphenyl)carbamic acid tert-butyl ester

: 1195781-45-3
tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / dimethyl sulfoxide / 4 h / 20 °C

2: hydrogen / 5%-palladium/activated carbon / methanol / 8 h / 20 °C

3: bromine / acetic acid / 0 - 20 °C

With hydrogen; bromine; caesium carbonate; 5%-palladium/activated carbon; In methanol; acetic acid; dimethyl sulfoxide;

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 1195781-45-3
tert-butyl {4-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-3-fluorophenyl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / dimethyl sulfoxide / 4 h / 20 °C

2: hydrogen / 5%-palladium/activated carbon / methanol / 8 h / 20 °C

3: bromine / acetic acid / 0 - 20 °C

With hydrogen; bromine; caesium carbonate; 5%-palladium/activated carbon; In methanol; acetic acid; dimethyl sulfoxide;