methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

Base Information

Chemical Name:methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate
CAS No.:850317-92-9
Molecular Formula:C₂₂H₂₉ClN₂O₇S
Molecular Weight:501
Hs Code.:

Synonyms:methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

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Chemical Property of methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

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Technology Process of methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

There total 4 articles about methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate 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: 64.0%

: 850317-91-8
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-(3-chloro-4-iodophenyl)propanoate

: 119639-24-6
2-tert-butylisothiazol-3(2H)-one 1,1-dioxide

: 850317-92-9
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

Guidance literature:: With tetrabutyl-ammonium chloride; palladium diacetate; triethylamine; In N,N-dimethyl-formamide; at 65 ℃; for 2h;
DOI:10.1021/jm0600904

Reference yield:

: 850317-90-7
methyl (2S)-3-(4-amino-3-chlorophenyl)-2-[(tert-butoxycarbonyl)amino]propanoate

: 850317-92-9
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: aq. hydrochloric acid; sodium nitrite / 0.5 h / 0 °C

1.2: 2.1 g / aq. potassium iodide / 0.67 h / 20 - 35 °C

2.1: 64 percent / tetra-N-butylammonium chloride; palladium acetate; triethylamine / dimethylformamide / 2 h / 65 °C

With hydrogenchloride; tetrabutyl-ammonium chloride; palladium diacetate; triethylamine; sodium nitrite; In N,N-dimethyl-formamide; 2.1: Heck reaction;
DOI:10.1021/jm0600904

Reference yield:

: 65615-90-9
(S)-methyl 3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoate

: 850317-92-9
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(2-tert-butyl-1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)-3-chlorophenyl]propanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 645 mg / N-chlorosuccinimide / dimethylformamide / 24 h

2.1: aq. hydrochloric acid; sodium nitrite / 0.5 h / 0 °C

2.2: 2.1 g / aq. potassium iodide / 0.67 h / 20 - 35 °C

3.1: 64 percent / tetra-N-butylammonium chloride; palladium acetate; triethylamine / dimethylformamide / 2 h / 65 °C

With hydrogenchloride; N-chloro-succinimide; tetrabutyl-ammonium chloride; palladium diacetate; triethylamine; sodium nitrite; In N,N-dimethyl-formamide; 3.1: Heck reaction;
DOI:10.1021/jm0600904