(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

Base Information

Chemical Name:(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid
CAS No.:1609399-00-9
Molecular Formula:C₁₇H₁₄F₃NO₄S
Molecular Weight:385.364
Hs Code.:

Synonyms:(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

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Chemical Property of (+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

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Technology Process of (+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

There total 6 articles about (+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic 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: 89.0%

: 1609398-93-7
(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazinyl]acetic acid isopropyl ester

: 1609399-00-9
(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; water; at 20 ℃; for 12h;
DOI:10.1021/jo500338c

Reference yield: 75.0%

: C₂₅H₂₃F₃N₂O₃S

: 1609399-00-9
(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; water; for 10h; Reflux;
DOI:10.3109/14756366.2014.961447

Reference yield:

: (Z)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid isopropyl ester

: 1609399-00-9
(+)-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxido-3,4-dihydro-2H-1,2-benzothiazin-4-yl]acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: (R)-tol-BINAP; sodium t-butanolate; copper diacetate; diphenylsilane / tetrahydrofuran / 0 - 20 °C / Schlenk technique; Inert atmosphere; Glovebox

2: hydrogenchloride / water; 1,4-dioxane / 12 h / 20 °C

With hydrogenchloride; diphenylsilane; copper diacetate; (R)-tol-BINAP; sodium t-butanolate; In tetrahydrofuran; 1,4-dioxane; water;
DOI:10.1021/jo500338c