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

Base Information

Chemical Name:5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylic acid hydrochloride
CAS No.:1041609-79-3
Molecular Formula:C₂₃H₂₂F₃N₃O₆S*ClH
Molecular Weight:561.966
Hs Code.:

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

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

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

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

Reference yield:

: C₂₈H₃₀F₃N₃O₈S

: 1041609-79-3
5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylic acid 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

: 1041609-79-3
5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylic acid 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

: 1041609-79-3
5-((3-((R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxamido)methyl)benzo[d][1,3]dioxol-2-carboxylic acid 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