(R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

Base Information

Chemical Name:(R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid
CAS No.:1071471-17-4
Molecular Formula:C₂₂H₂₂N₆O₆S₃
Molecular Weight:562.651
Hs Code.:

Synonyms:(R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

There total 6 articles about (R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid 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: 63.0%

: 1071472-23-5
(R)-methyl 3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoate

: 1071471-17-4
(R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

Guidance literature:: With lithium hydroxide; water; In tetrahydrofuran; at 100 ℃; for 0.166667h; Microwave irradiation;

Reference yield:

: 452-35-7
6-ethoxybenzothiazole-2-sulfonamide

: 1071471-17-4
(R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: aluminum (III) chloride / dichloromethane / 24 h / 0 - 20 °C

2.1: sodium hydroxide / methanol; N,N-dimethyl-formamide / 0.75 h / 23 °C

2.2: 2.5 h

3.1: copper(II) sulfate; sodium L-ascorbate / water; tert-butyl alcohol / 24 h / 20 °C / pH 7.4 / Aqueous phosphate buffer

4.1: lithium hydroxide; water / tetrahydrofuran / 0.17 h / 100 °C / Microwave irradiation

With aluminum (III) chloride; lithium hydroxide; sodium hydroxide; water; copper(II) sulfate; sodium L-ascorbate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 29927-14-8
6-hydroxy-2-benzothiazolesulfonamide

: 1071471-17-4
(R)-3-(benzylthio)-2-(2-(4-((2-sulfamoylbenzo[d]thiazol-6-yloxy)methyl)-1H-1,2,3-triazol-1-yl)acetamido)propanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / methanol; N,N-dimethyl-formamide / 0.75 h / 23 °C

1.2: 2.5 h

2.1: copper(II) sulfate; sodium L-ascorbate / water; tert-butyl alcohol / 24 h / 20 °C / pH 7.4 / Aqueous phosphate buffer

3.1: lithium hydroxide; water / tetrahydrofuran / 0.17 h / 100 °C / Microwave irradiation

With lithium hydroxide; sodium hydroxide; water; copper(II) sulfate; sodium L-ascorbate; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; tert-butyl alcohol;