2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

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Chemical Name:2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide
CAS No.:848431-85-6
Molecular Formula:C₂₃H₁₈F₃N₅O₂S
Molecular Weight:485.489
Hs Code.:

Synonyms:2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

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Chemical Property of 2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

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Technology Process of 2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

There total 5 articles about 2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide 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: 59.0%

: 848422-70-8
C₁₄H₇ClF₃N₃O

: 4815-28-5
2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

: 848431-85-6
2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1021/jm500300r

Reference yield:

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 848431-85-6
2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: morpholine; sulfur / ethanol / 60 °C

2: pyridine / dichloromethane / 16 h / 20 °C

With morpholine; pyridine; sulfur; In ethanol; dichloromethane;
DOI:10.1021/jm500300r

Reference yield:

: 326-06-7
1-Phenyl-4,4,4-trifluorobutane-1,3-dione

: 848431-85-6
2-({[5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]-carbonyl}amino)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid / Reflux

2: alkali hydroxide / ethanol; water / 3 h / Reflux

3: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 2 h / 20 °C

4: pyridine / dichloromethane / 16 h / 20 °C

With pyridine; oxalyl dichloride; acetic acid; N,N-dimethyl-formamide; In ethanol; dichloromethane; water;
DOI:10.1021/jm500300r