4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

Base Information

Chemical Name:4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine
CAS No.:1341127-08-9
Molecular Formula:C₂₁H₂₇N₃O₄S
Molecular Weight:417.529
Hs Code.:

Synonyms:4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

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Chemical Property of 4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

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Technology Process of 4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

There total 6 articles about 4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine 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: 100.0%

: 110-91-8,99108-56-2
morpholine

: 1341127-10-3
2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl methanesulfonate

: 1341127-08-9
4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

Guidance literature:: With sodium hydrogencarbonate; In ethanol; Reflux;
DOI:10.1016/j.bmc.2011.08.054

Reference yield:

: 1341126-59-7
2-(3-phenoxybenzyl)-1,2,5-thiadiazolidine 1,1-dioxide

: 1341127-08-9
4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 °C

1.2: 20 °C

2.1: lithium borohydride; ethanol / tetrahydrofuran / 20 °C

2.2: pH 4

3.1: triethylamine / dichloromethane / 0 - 20 °C

4.1: sodium hydrogencarbonate / ethanol / Reflux

With lithium borohydride; ethanol; sodium hydride; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.08.054

Reference yield:

: 1341126-95-1
methyl [5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]acetate

: 1341127-08-9
4-{2-[5-(3-phenoxybenzyl)-1,1-dioxido-1,2,5-thiadiazolidin-2-yl]ethyl}morpholine

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium borohydride; ethanol / tetrahydrofuran / 20 °C

1.2: pH 4

2.1: triethylamine / dichloromethane / 0 - 20 °C

3.1: sodium hydrogencarbonate / ethanol / Reflux

With lithium borohydride; ethanol; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/j.bmc.2011.08.054