4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

Base Information

Chemical Name:4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid
CAS No.:1135689-24-5
Molecular Formula:C₄₀H₅₀F₃N₅O₁₀
Molecular Weight:817.86
Hs Code.:

4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

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Chemical Property of 4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

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Technology Process of 4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

There total 8 articles about 4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid 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:

: 108-30-5
succinic acid anhydride

: 1631962-23-6
C₃₆H₄₆F₃N₅O₇*ClH

: 1135689-24-5
4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1039/c4ob00962b

Reference yield:

: 1616606-78-0
tert-butyl N-[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamate

: 1135689-24-5
4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

3: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

4: N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

5: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

6: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1039/c4ob00962b

Reference yield:

: 1616606-79-1
tert-butyl N-[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamate

: 1135689-24-5
4-[[(1S)-1-[[(1S)-1-[[(1S)-1-[[(1S)-1-[(4-hydroxyphenyl)methyl]-2-oxo-2-[[2-oxo-4-(trifluoromethyl)chromen-7-yl]amino]ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-butyl]amino]-4-oxo-butanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

3: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

4: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1039/c4ob00962b