(S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride

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Chemical Name:(S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride
CAS No.:110206-11-6
Molecular Formula:C₂₂H₃₈N₄O₂S*2ClH
Molecular Weight:495.557
Hs Code.:

Synonyms:(S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride

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Chemical Property of (S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride

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Technology Process of (S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride

There total 12 articles about (S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride 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:

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

: 110206-11-6
(S)-2-Amino-N-((1S,2S)-1-cyclohexylmethyl-3-cyclohexylsulfanyl-2-hydroxy-propyl)-3-(1H-imidazol-4-yl)-propionamide; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1-hydroxybenzotriazole monohydrate (HOBt), N-methylmorpholine, 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / dimethylformamide / -23 - 20 °C

2: HCl / ethanol / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00394a035

Reference yield:

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

: 110206-11-6
(2R,3S)-3-(histidylamino)-4-cyclohexyl-1-(cyclohexylthio)-2-hydroxybutane dihydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1-hydroxybenzotriazole monohydrate (HOBt), N-methylmorpholine, 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / dimethylformamide / -23 - 20 °C

2: HCl / ethanol / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00394a035