tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

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Chemical Name:tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate
CAS No.:1620011-02-0
Molecular Formula:C₃₄H₃₈F₂N₆O₅S
Molecular Weight:680.776
Hs Code.:

Synonyms:tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

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Chemical Property of tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

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Technology Process of tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

There total 6 articles about tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}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: 91.0%

: 26189-59-3
1-chloro-1-(dimethylamino)-2-methyl-1-propene

: 1270034-25-7
5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazole-4-carboxylic acid

: 1620010-99-2
tert-butyl [(3S)-1-(3-aminoquinolin-4-yl)piperidin-3-yl]carbamate

: 1620011-02-0
tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

Guidance literature:: 1-chloro-1-(dimethylamino)-2-methyl-1-propene; 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazole-4-carboxylic acid; In tetrahydrofuran; at 20 - 30 ℃; for 5h;

tert-butyl [(3S)-1-(3-aminoquinolin-4-yl)piperidin-3-yl]carbamate; With pyridine; In tetrahydrofuran; at 20 - 30 ℃; for 2h;

Reference yield:

: 39061-97-7
4-chloro-3-nitroquinoline

: 1620011-02-0
tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 2 h / 100 °C / Microwave irradiation

2.1: iron; ammonium chloride / ethanol; water / 1 h / 80 °C

3.1: tetrahydrofuran / 5 h / 20 - 30 °C

3.2: 2 h / 20 - 30 °C

With iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; water; butan-1-ol;

Reference yield:

: 1620011-00-8
methyl 2-bromo-5-[(tert-butoxycarbonyl)amino]-1,3-thiazole-4-carboxylate

: 1620011-02-0
tert-butyl {(3S)-1-[3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluorophenyl)-1,3-thiazol-4-yl]carbonyl}amino)quinolin-4-yl]piperidin-3-yl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: bis(tri-t-butylphosphine)palladium⁽⁰⁾; N-ethyl-N,N-diisopropylamine / water; 1,4-dioxane / 1 h / 100 °C / Inert atmosphere

2.1: lithium hydroxide monohydrate / water; methanol / 5 h / 60 °C

3.1: tetrahydrofuran / 5 h / 20 - 30 °C

3.2: 2 h / 20 - 30 °C

With bis(tri-t-butylphosphine)palladium⁽⁰⁾; lithium hydroxide monohydrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; methanol; water;