N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

Base Information

Chemical Name:N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide
CAS No.:1448150-24-0
Molecular Formula:C₂₅H₃₂N₂O₂
Molecular Weight:392.541
Hs Code.:

Synonyms:N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

Suppliers and Price of N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

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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-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

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Technology Process of N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

There total 1 articles about N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide 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: 86.0%

: 119072-55-8,7188-38-7
tert-butylisonitrile

: 5962-81-2
4-cyclohexyl-2-butynoic acid

: 100-52-7
benzaldehyde

: 2450-71-7
Propargylamine

: 1448150-24-0
N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

Guidance literature:: With sodium sulfate; In methanol; at 20 ℃; Inert atmosphere;
DOI:10.1039/c3cc43418d

Reference yield: 65.0%

: 1448150-24-0
N-((tert-butylcarbamoyl)(phenyl)methyl)-4-cyclohexyl-N-(prop-2-ynyl)but-2-ynamide

: 1448150-44-4
N-(tert-butyl)-2-(3'-oxospiro[cyclohexane-1,6'-cyclopenta[c]pyridin]-2'(1'H,3'H,5'H)-yl)-2-phenylacetamide

Guidance literature:: With chloro(1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene)gold(I); silver trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 120 ℃; regioselective reaction; Inert atmosphere;
DOI:10.1039/c3cc43418d