(S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

Base Information

Chemical Name:(S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide
CAS No.:1446513-26-3
Molecular Formula:C₂₂H₂₁N₃O₉S
Molecular Weight:503.489
Hs Code.:

Synonyms:(S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

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Chemical Property of (S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

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Technology Process of (S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

There total 4 articles about (S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide 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:

: 1446512-96-4
(S)-4-(4-(2-amino-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide hydrochloride

: 2937-50-0
Allyl chloroformate

: 1446513-26-3
(S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; for 1h;
DOI:10.1039/c3ob41047a

Reference yield:

: 66074-00-8
3,4-bis(phenylsulfonyl)-1,2,5-oxadiazole 2-oxide

: 1446513-26-3
(S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h / 20 °C

2: hydrogenchloride / dichloromethane; 1,4-dioxane; water

3: triethylamine / tetrahydrofuran / 1 h / 0 - 20 °C

With hydrogenchloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;
DOI:10.1039/c3ob41047a

Reference yield:

: 4326-36-7
(S)-N-(tert-butoxycarbonyl)tyrosine methyl ester

: 1446513-26-3
(S)-4-(4-(2-((allyloxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h / 20 °C

2: hydrogenchloride / dichloromethane; 1,4-dioxane; water

3: triethylamine / tetrahydrofuran / 1 h / 0 - 20 °C

With hydrogenchloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;
DOI:10.1039/c3ob41047a