1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

Base Information

Chemical Name:1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane
CAS No.:502761-25-3
Molecular Formula:C₂₉H₄₆N₄O₆
Molecular Weight:546.707
Hs Code.:

Synonyms:1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

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Chemical Property of 1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

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Technology Process of 1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

There total 8 articles about 1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane 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: 26.0%

: 68076-36-8
1-amino-4-[(tert-butyloxycarbonyl)amino]butane

: 658053-31-7
N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-proline

: 502761-25-3
1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

Guidance literature:: N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-proline; With diisopropyl-carbodiimide; In dichloromethane; at 0 ℃; for 0.5h;

1-amino-4-[(tert-butyloxycarbonyl)amino]butane; In dichloromethane;

Reference yield:

: 34071-95-9
N-succinimidyl-3-(p-hydroxyphenyl)propionate

: 502761-25-3
1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

Guidance literature:: Multi-step reaction with 4 steps

1.1: 76 percent / NaHCO₃ / ethanol; H₂O / 16 h / 20 °C

2.1: 84 percent / dicyclohexylcarbodiimide / ethyl acetate / 16 h / 0 - 20 °C

3.1: 1.87 g / aq. LiOH / 1,2-dimethoxy-ethane / 2 h / 20 °C

4.1: diisopropylcarbodiimide / CH₂Cl₂ / 1 h / cooling

4.2: 26 percent / CH₂Cl₂ / 48 h

With lithium hydroxide; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; diisopropyl-carbodiimide; In 1,2-dimethoxyethane; ethanol; dichloromethane; water; ethyl acetate;
DOI:10.1002/ardp.200300726

Reference yield:

: 501-97-3
4-hydroxyphenylpropionic acid

: 502761-25-3
1-tert-butoxycarbonylamino-4-{N-[3-(4-hydroxyphenyl)propionyl]-L-isoleucyl-L-prolylamino}butane

Guidance literature:: Multi-step reaction with 5 steps

1.1: 78 percent / dicyclohexylcarbodiimide / ethyl acetate / 16 h

2.1: 76 percent / NaHCO₃ / ethanol; H₂O / 16 h / 20 °C

3.1: 84 percent / dicyclohexylcarbodiimide / ethyl acetate / 16 h / 0 - 20 °C

4.1: 1.87 g / aq. LiOH / 1,2-dimethoxy-ethane / 2 h / 20 °C

5.1: diisopropylcarbodiimide / CH₂Cl₂ / 1 h / cooling

5.2: 26 percent / CH₂Cl₂ / 48 h

With lithium hydroxide; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; diisopropyl-carbodiimide; In 1,2-dimethoxyethane; ethanol; dichloromethane; water; ethyl acetate;
DOI:10.1002/ardp.200300726