methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

Base Information

Chemical Name:methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate
CAS No.:1085784-06-0
Molecular Formula:C₂₄H₂₀F₃N₅O₄S
Molecular Weight:531.515
Hs Code.:

Synonyms:methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

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Chemical Property of methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

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Technology Process of methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

There total 7 articles about methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate 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:

: 1085784-05-9
methyl 6-({[(4-amino-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-1,3-thiazol-5-yl)carbonyl]amino}carbonyl)nicotinate

: 1085784-06-0
methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

Guidance literature:: methyl 6-({[(4-amino-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-1,3-thiazol-5-yl)carbonyl]amino}carbonyl)nicotinate; With camphor-10-sulfonic acid; In xylene; for 2h; Heating / reflux;

With sodium hydrogencarbonate; In water; xylene;

Reference yield:

: 444-30-4
2-(trifluoromethyl)phenol

: 1085784-06-0
methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 16 h / 0 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 10 h / 0 - 20 °C

3.1: ethanol / 0.5 h / Heating / reflux

4.1: ammonia; triethylamine / methanol / 20 °C

5.1: oxalyl dichloride / N,N-dimethyl-formamide / toluene / 0.5 h / 20 °C

5.2: 72 h / 20 °C

6.1: camphor-10-sulfonic acid / xylene / 2 h / Heating / reflux

With oxalyl dichloride; camphor-10-sulfonic acid; ammonia; triethylamine; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; xylene;

Reference yield:

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1085784-06-0
methyl 6-(7-oxo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}-6,7-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl)nicotinate

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 16 h / 0 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 10 h / 0 - 20 °C

3.1: ethanol / 0.5 h / Heating / reflux

4.1: ammonia; triethylamine / methanol / 20 °C

5.1: oxalyl dichloride / N,N-dimethyl-formamide / toluene / 0.5 h / 20 °C

5.2: 72 h / 20 °C

6.1: camphor-10-sulfonic acid / xylene / 2 h / Heating / reflux

With oxalyl dichloride; camphor-10-sulfonic acid; ammonia; triethylamine; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; xylene;