(R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate

Base Information

Chemical Name:(R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate
CAS No.:1006706-48-4
Molecular Formula:C₂₀H₂₈F₃N₃O₃
Molecular Weight:415.456
Hs Code.:

Synonyms:(R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate

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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 (R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate

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Technology Process of (R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate

There total 1 articles about (R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate 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: 89.0%

: 1006706-47-3
(R)-benzyl 4-(3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)butanoyl)-1,4-diazepine-1-carboxylate

: 1006706-48-4
(R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 10h;
DOI:10.1016/j.bmcl.2008.10.076

Reference yield: 71.0%

: 1006706-48-4
(R)-tert-butyl 4-(1,4-diazepan-1-yl)-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate

: 1877-71-0
benzene 1,3-dicarboxylic acid monomethyl ester

: 1100227-62-0
(R)-methyl 3-(4-(3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)butanoyl)-1,4-diazepane-1-carbonyl)benzoate

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/j.bmcl.2008.10.076