N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

Base Information

Chemical Name:N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide
CAS No.:1303445-88-6
Molecular Formula:C₂₂H₁₅F₆N₅O
Molecular Weight:479.384
Hs Code.:

Synonyms:N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

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Technology Process of N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

There total 7 articles about N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-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: 14.0%

: 1303445-74-0
N-[3,5-bis(trifluoromethyl)benzyl]-6-chloro-2-methyl-4-phenylnicotinamide

: 1303445-88-6
N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

Guidance literature:: With sodium azide; In N,N-dimethyl-formamide; at 130 ℃; for 48h;
DOI:10.1016/j.bmc.2011.02.031

Reference yield:

: 14371-10-9
(E)-3-phenylpropenal

: 1303445-88-6
N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: piperidine / N,N-dimethyl-formamide / 1 h / Reflux

2.1: sodium hydroxide / ethanol / 6 h / Reflux

2.2: 0 - 5 °C / pH 5 - 6

3.1: thionyl chloride / 3 h / Reflux

4.1: triethylamine / dichloromethane / 1 h / Reflux

5.1: 3-chloro-benzenecarboperoxoic acid / chloroform / 4 h / 20 °C

6.1: trichlorophosphate / 3 h / Reflux

7.1: sodium azide / N,N-dimethyl-formamide / 48 h / 130 °C

With piperidine; thionyl chloride; sodium azide; triethylamine; 3-chloro-benzenecarboperoxoic acid; sodium hydroxide; trichlorophosphate; In ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.02.031

Reference yield:

: 1256643-39-6
2-methyl-4-phenylnicotinic acid

: 1303445-88-6
N-[3,5-bis(trifluoromethyl)benzyl]-5-methyl-7-phenyltetrazolo[1,5-a]pyridine-6-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: thionyl chloride / 3 h / Reflux

2: triethylamine / dichloromethane / 1 h / Reflux

3: 3-chloro-benzenecarboperoxoic acid / chloroform / 4 h / 20 °C

4: trichlorophosphate / 3 h / Reflux

5: sodium azide / N,N-dimethyl-formamide / 48 h / 130 °C

With thionyl chloride; sodium azide; triethylamine; 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; In dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.02.031