tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

Base Information

Chemical Name:tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate
CAS No.:229486-37-7
Molecular Formula:C₂₁H₃₂N₄O₅
Molecular Weight:420.509
Hs Code.:

Synonyms:tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

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Chemical Property of tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

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Technology Process of tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

There total 5 articles about tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate 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: 81.0%

: 7142-72-5
N-benzyloxamic acid ethyl ester

: 229486-30-0
(S)-tert-butyl (1-((2-aminoethyl)amino)-3-methyl-1-oxobutan-2-yl)carbamate

: 229486-37-7
tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

Guidance literature:: In methanol; chloroform; at 20 ℃; for 1h;

Reference yield:

: 58632-95-4
2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile

: 229486-37-7
tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N / dioxane

2: methanol / 20 °C

3: 81 percent / methanol; CHCl₃ / 1 h / 20 °C

With triethylamine; In 1,4-dioxane; methanol; chloroform; 1: Condensation / 2: Substitution / 3: Substitution;

Reference yield:

: 6306-52-1
L-valine methylester hydrochloride

: 229486-37-7
tert-butyl 3-isopropyl-4,9,10-trioxo-12-phenyl-2,5,8,11-tetraazadodecanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N / dioxane

2: methanol / 20 °C

3: 81 percent / methanol; CHCl₃ / 1 h / 20 °C

With triethylamine; In 1,4-dioxane; methanol; chloroform; 1: Condensation / 2: Substitution / 3: Substitution;