methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Base Information

Chemical Name:methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide
CAS No.:1446282-83-2
Molecular Formula:C₁₆H₁₁F₄NO₅S
Molecular Weight:405.327
Hs Code.:

Synonyms:methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

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Chemical Property of methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

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Technology Process of methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

There total 4 articles about methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide 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:

: 1446282-69-4
methyl (S)-2-(4-methoxyphenyl)-2-(2,3,4,5,6-pentafluorophenylsulfonamido)acetate

: 1446282-83-2
methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

: 1446282-84-3
methyl (S)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Guidance literature:: With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,2-dimethoxyethane; at 0 - 25 ℃; for 96h; Overall yield = 99 %; Overall yield = 401 mg; enantioselective reaction;
DOI:10.1021/ol401557v

Reference yield:

: 183671-61-6
(S)-tert-butoxycarbonylamino(4-methoxyphenyl)acetic acid methyl ester

: 1446282-83-2
methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

: 1446282-84-3
methyl (S)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Guidance literature:: Multi-step reaction with 3 steps

1: chloroform / 4 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 0 - 25 °C

3: N,N,N′,N′-tetramethyl-N″-tert-butylguanidine / 1,2-dimethoxyethane / 0 - 25 °C

With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; N-ethyl-N,N-diisopropylamine; In 1,2-dimethoxyethane; dichloromethane; chloroform;
DOI:10.1021/ol401557v

Reference yield:

: 69651-48-5
N-tert-butyloxycarbonyl-L-4-hydroxyphenylglycine

: 1446282-83-2
methyl (R)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

: 1446282-84-3
methyl (S)-4,5,6,7-tetrafluoro-3-(4-methoxyphenyl)-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Guidance literature:: Multi-step reaction with 4 steps

1: aluminum (III) chloride / methanol; diethyl ether / 4 h / 0 - 20 °C

2: chloroform / 4 h / 0 - 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 0 - 25 °C

4: N,N,N′,N′-tetramethyl-N″-tert-butylguanidine / 1,2-dimethoxyethane / 0 - 25 °C

With aluminum (III) chloride; N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; N-ethyl-N,N-diisopropylamine; In methanol; 1,2-dimethoxyethane; diethyl ether; dichloromethane; chloroform;
DOI:10.1021/ol401557v