tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

Base Information

Chemical Name:tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate
CAS No.:1654765-81-7
Molecular Formula:C₃₈H₄₉N₅O₅
Molecular Weight:655.838
Hs Code.:

Synonyms:tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

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Chemical Property of tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

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Technology Process of tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

There total 5 articles about tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-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: 45.0%

: 1621105-14-3
methyl (S)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoate

: 124-40-3
dimethyl amine

: 1654765-81-7
tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

Guidance literature:: In methanol; at 50 ℃; for 48h;
DOI:10.1016/j.ejmech.2014.06.026

Reference yield:

: 3612-20-2
1-phenylmethyl-4-piperidone

: 1654765-81-7
tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: methanol / 96 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: methanol / 48 h / 50 °C

In methanol; 1.1: |Ugi Condensation;
DOI:10.1016/j.ejmech.2014.06.026

Reference yield:

: 59768-74-0,124184-67-4
(S)-2-t-butoxycarbonylaminosuccinic acid 4-methyl ester

: 1654765-81-7
tert-butyl (S)-(1-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-(dimethylamino)-1,4-dioxobutan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: methanol / 96 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: methanol / 48 h / 50 °C

In methanol; 1.1: |Ugi Condensation;
DOI:10.1016/j.ejmech.2014.06.026