(E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

Base Information

Chemical Name:(E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol
CAS No.:1416732-76-7
Molecular Formula:C₁₉H₁₅F₄N₉O
Molecular Weight:461.381
Hs Code.:

Synonyms:(E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

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Chemical Property of (E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

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Technology Process of (E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

There total 5 articles about (E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol 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:

: 76457-32-4
1-N-allyltetrazole

: 1416732-19-8,1443429-65-9
1-(5-bromopyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

: 1416732-76-7
(E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

Guidance literature:: With N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; palladium diacetate; In N,N-dimethyl-formamide; at 110 ℃; for 0.25h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 624-28-2
2,5-dibromopyridine

: 1416732-76-7
(E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

Guidance literature:: Multi-step reaction with 5 steps

1.1: copper / dimethyl sulfoxide / 1 h / 20 °C

1.2: 15 h / 20 °C

2.1: n-butyllithium / hexane; diethyl ether / -70 - 20 °C

3.1: diethyl ether / 0 - 20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 60 °C

5.1: N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine / palladium diacetate / N,N-dimethyl-formamide / 0.25 h / 110 °C / Inert atmosphere; Microwave irradiation

With n-butyllithium; copper; potassium carbonate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; palladium diacetate; In diethyl ether; hexane; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 294181-95-6
2-(5-bromopyridine-2-yl)-2,2-difluoroacetic acid ethyl ester

: 1416732-76-7
(E)-1-(5-(3-(1H-tetrazol-1-yl)prop-1-en-1-yl)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1: n-butyllithium / hexane; diethyl ether / -70 - 20 °C

2: diethyl ether / 0 - 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / 3 h / 60 °C

4: N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine / palladium diacetate / N,N-dimethyl-formamide / 0.25 h / 110 °C / Inert atmosphere; Microwave irradiation

With n-butyllithium; potassium carbonate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; palladium diacetate; In diethyl ether; hexane; N,N-dimethyl-formamide;