N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

Base Information

Chemical Name:N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene
CAS No.:110613-90-6
Molecular Formula:C₂₉H₄₉N₅O₅
Molecular Weight:547.739
Hs Code.:

N-<N-<(tert-butyloxy)carbonyl>-L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

Synonyms:N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

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Chemical Property of N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

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Technology Process of N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

There total 4 articles about N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene 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: 76.0%

: 110613-89-3
(4S,5S)-N-(3-Methylbutyl)-5-amino-4-hydroxy-6-cyclohexylhex-1-ene-2-carboxamide Hydrochloride

: 17791-52-5
N-(tert-butoxycarbonyl)-L-histidine

: 110613-90-6
N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at -23 - 20 ℃;
DOI:10.1021/jm00394a008

Reference yield:

: 98105-42-1
(S)-2-(t-butoxycarbonylamino)-3-cyclohexyl-1-propanal

: 110613-90-6
N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) n-butyllithium, 2.) ClTi(O-iPr)3

2: HCl(g) / dioxane / 1 h / Ambient temperature

3: 76 percent / 1-hydroxybenzotriazole*H₂O, 4-methylmorpholine, 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide*HCl / dimethylformamide / -23 - 20 °C

With 4-methyl-morpholine; triisopropoxytitanium(IV) chloride; hydrogenchloride; n-butyllithium; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/jm00394a008

Reference yield:

: 110613-29-1
N-isopentylmethacrylamide

: 110613-90-6
N--L-histidyl>-5(S)-amino-6-cyclohexyl-4(S)-hydroxy-2-(N-isopentylcarbamoyl)hex-1-ene

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) n-butyllithium, 2.) ClTi(O-iPr)3

2: HCl(g) / dioxane / 1 h / Ambient temperature

3: 76 percent / 1-hydroxybenzotriazole*H₂O, 4-methylmorpholine, 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide*HCl / dimethylformamide / -23 - 20 °C

With 4-methyl-morpholine; triisopropoxytitanium(IV) chloride; hydrogenchloride; n-butyllithium; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/jm00394a008