(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

Base Information

Chemical Name:(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid
CAS No.:1580457-44-8
Molecular Formula:C₁₇H₁₉ClN₂O₄S
Molecular Weight:382.868
Hs Code.:

Synonyms:(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

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Chemical Property of (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

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Technology Process of (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

There total 6 articles about (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)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:

: 24424-99-5
di-tert-butyl dicarbonate

: C₁₂H₁₁ClN₂O₂S

: 1580457-44-8
(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; pH=8 - 9;
DOI:10.1002/ejoc.201501495

Reference yield:

: 17969-22-1
4-chloromethyl-2-(4-chloro-phenyl)-thiazole

: 1580457-44-8
(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium iodide / 1 h / Reflux

2.1: lithium diisopropyl amide / tetrahydrofuran; hexane / 0.5 h / -78 °C

2.2: 14 h / -78 - -10 °C

3.1: citric acid / water; tetrahydrofuran / 72 h / 20 °C

4.1: trifluoroacetic acid; chlorotriisopropylsilane / 4 h / 20 °C

5.1: sodium hydrogencarbonate / water; tetrahydrofuran / 20 °C / pH 8 - 9

With chlorotriisopropylsilane; sodium hydrogencarbonate; trifluoroacetic acid; citric acid; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; hexane; water;
DOI:10.1002/ejoc.201501495

Reference yield:

: C₁₆H₁₉ClN₂O₂S

: 1580457-44-8
(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-(4-chlorophenyl)thiazol-4-yl)propanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid; chlorotriisopropylsilane / 4 h / 20 °C

2: sodium hydrogencarbonate / water; tetrahydrofuran / 20 °C / pH 8 - 9

With chlorotriisopropylsilane; sodium hydrogencarbonate; trifluoroacetic acid; In tetrahydrofuran; water;
DOI:10.1002/ejoc.201501495