but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

Base Information

Chemical Name:but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate
CAS No.:1346110-70-0
Molecular Formula:C₁₉H₁₇N₇O₃
Molecular Weight:391.389
Hs Code.:

Synonyms:but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

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Chemical Property of but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

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Technology Process of but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

There total 4 articles about but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-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: 92.0%

: 1354047-17-8
but-3-yn-1-yl {6-[({[(Z)-cyano(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

: 1346110-70-0
but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

Guidance literature:: With sodium azide; triethylamine hydrochloride; In N,N-dimethyl-formamide; at 60 ℃; for 12h;

Reference yield:

: 140-29-4
phenylacetonitrile

: 1346110-70-0
but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide; isopentyl nitrite / ethanol / 15 °C

2: potassium iodide / N,N-dimethyl-formamide; acetonitrile / 7 h / 20 °C

3: sodium azide; triethylamine hydrochloride / N,N-dimethyl-formamide / 12 h / 60 °C

With sodium azide; triethylamine hydrochloride; potassium iodide; sodium hydroxide; isopentyl nitrite; In ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: sodium {[(Z)-cyano(phenyl)methylene]amino}oxidanide

: 1346110-70-0
but-3-yn-1-yl {6-[({[(Z)-phenyl(1H-tetrazol-5-yl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium iodide / N,N-dimethyl-formamide; acetonitrile / 7 h / 20 °C

2: sodium azide; triethylamine hydrochloride / N,N-dimethyl-formamide / 12 h / 60 °C

With sodium azide; triethylamine hydrochloride; potassium iodide; In N,N-dimethyl-formamide; acetonitrile;