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(3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride

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  • Chemical Name:(3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride
  • CAS No.:1311319-11-5
  • Molecular Formula:C25H27F3N4O6S*ClH
  • Molecular Weight:605.035
  • Hs Code.:
  • Mol file:1311319-11-5.mol
(3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride

Synonyms:(3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride

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Chemical Property of (3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride Edit
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Technology Process of (3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride

There total 6 articles about (3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid 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:
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran / 0.33 h / 20 °C
1.2: 4 h / 20 °C
2.1: dmap; triethylamine; HATU / N,N-dimethyl-formamide / 20 °C
3.1: hydrogenchloride / ethyl acetate; 1,4-dioxane / 20 °C
With hydrogenchloride; dmap; sodium hydride; triethylamine; HATU; In tetrahydrofuran; 1,4-dioxane; ethyl acetate; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 4 steps
1.1: tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; tetra-(n-butyl)ammonium iodide; tetraethylammonium iodide / toluene / 12 h / Reflux
2.1: sodium hydride / tetrahydrofuran / 0.33 h / 20 °C
2.2: 4 h / 20 °C
3.1: dmap; triethylamine; HATU / N,N-dimethyl-formamide / 20 °C
4.1: hydrogenchloride / ethyl acetate; 1,4-dioxane / 20 °C
With hydrogenchloride; dmap; tetraethylammonium iodide; tetra(n-butyl)ammonium hydrogensulfate; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; triethylamine; HATU; In tetrahydrofuran; 1,4-dioxane; ethyl acetate; N,N-dimethyl-formamide; toluene;
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