2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

Base Information

Chemical Name:2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate
CAS No.:1186301-41-6
Molecular Formula:C₅₈H₆₉N₃O₈S
Molecular Weight:968.267
Hs Code.:

2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

Synonyms:2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

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Chemical Property of 2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

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Technology Process of 2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

There total 1 articles about 2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate 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:

: 242460-24-8
6-amino-1-[bis(4-methoxyphenyl)(phenyl)methoxy]hexane-2-ol

: 804551-46-0
C₃₅H₄₁N₃O₇S

: 1186301-41-6
2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 25 ℃; for 0.333333h;
DOI:10.2174/157017809787003160

Reference yield: 90.0%

: 108-30-5
succinic acid anhydride

: 1186301-41-6
2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

: 1186301-46-1
2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-[(3-carboxypropanoyl)oxy]hexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

Guidance literature:: With dmap; In pyridine; at 25 ℃; for 12h;
DOI:10.2174/157017809787003160

Reference yield: 86.0%

: 1186301-41-6
2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

: 102691-36-1
N,N,N',N'-tetraisopropyl 2-cyanoethylphosphorodiamidite

: 1186301-43-8
2-((1E,3Z)-3-{1-[12-{[bis(4-methoxyphenyl)(phenyl)methoxy]methyl}-17-cyano-14-(diisopropylamino)-6-oxo-13,15-dioxa-7-aza-14-phosphaheptadec-1-yl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate

Guidance literature:: 2-((1E,3Z)-3-{1-[6-({6-[bis(4-methoxyphenyl)(phenyl)methoxy]-5-hydroxyhexyl}amino)-6-oxohexyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene}prop-1-en-1-yl)-1-ethyl-3,3-dimethyl-3H-indolium-5-sulfonate; With 1H-tetrazole; In pyridine; acetonitrile; at 25 ℃; for 0.5h; Molecular sieve;

N,N,N',N'-tetraisopropyl 2-cyanoethylphosphorodiamidite; In pyridine; acetonitrile; at 25 ℃; for 0.25h; Molecular sieve;
DOI:10.2174/157017809787003160