ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

Base Information

Chemical Name:ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride
CAS No.:1041609-78-2
Molecular Formula:C₂₅H₂₆F₃N₃O₆S*ClH
Molecular Weight:590.02
Hs Code.:

ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

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Chemical Property of ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

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Technology Process of ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

There total 5 articles about ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate 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:

: C₃₀H₃₄F₃N₃O₈S

: 1041609-78-2
ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

Guidance literature:: With hydrogenchloride; water; In ethyl acetate; at 20 ℃; for 12h;
DOI:10.1016/j.bmcl.2011.01.041

Reference yield:

: 1283679-05-9
C₂₁H₂₇F₃N₂O₅S

: 1041609-78-2
ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: water; lithium hydroxide / tetrahydrofuran / 12 h / 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12 h / 20 °C

3: hydrogenchloride; water / ethyl acetate / 12 h / 20 °C

With hydrogenchloride; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2011.01.041

Reference yield:

: 1041611-84-0
3-[(R)-3-t-butoxycarbonylamino-4-(2,4,5-trifluorophenyl)-butyryl]-thiazolidine-2-carboxylic acid

: 1041609-78-2
ethyl 5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylate hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12 h / 20 °C

2: hydrogenchloride; water / ethyl acetate / 12 h / 20 °C

With hydrogenchloride; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2011.01.041