methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

Base Information

Chemical Name:methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate
CAS No.:959992-00-8
Molecular Formula:C₃₄H₄₀Cl₂N₄O₅
Molecular Weight:655.621
Hs Code.:

Synonyms:methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

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Chemical Property of methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

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Technology Process of methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

There total 2 articles about methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate 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: 22.0%

: 959991-98-1
tert-butyl methyl[6-(piperidin-4-ylmethyl)pyridin-2-yl]carbamate

: 959991-99-2
methyl (S)-2-(2,6-dichlorobenzamido)-3-(4-iodophenyl)propanoate

: 959992-00-8
methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

Guidance literature:: With copper(l) iodide; caesium carbonate; L-proline; In dimethyl sulfoxide; at 90 ℃; for 18h;

Reference yield:

: 959991-97-0
benzyl 4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidine-1-carboxylate

: 959992-00-8
methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / ethanol / 1.5 h / 2068.65 Torr

2: copper(l) iodide; caesium carbonate; L-proline / dimethyl sulfoxide / 18 h / 90 °C

With copper(l) iodide; hydrogen; caesium carbonate; L-proline; palladium 10% on activated carbon; In ethanol; dimethyl sulfoxide;

Reference yield: 84.0%

: 959992-00-8
methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate

: methyl N-(2,6-dichlorobenzoyl)-4-(4-{[6-(methylamino)pyridin-2-yl]methyl}piperidin-1-yl)-L-phenylalaninate

Guidance literature:: methyl 4-[4-({6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}methyl)piperidin-1-yl]-N-(2,6-dichlorobenzoyl)-L-phenylalaninate; With trifluoroacetic acid; at 20 ℃; for 2h;

With ammonia; In methanol; dichloromethane;