4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

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Chemical Name:4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol
CAS No.:1442372-01-1
Molecular Formula:C₂₈H₃₀N₆O₅S
Molecular Weight:562.649
Hs Code.:

Synonyms:4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

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Chemical Property of 4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

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Technology Process of 4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

There total 5 articles about 4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol 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: 82.0%

: 1442371-98-3
10-(2-{[tert-butyl(diphenyl)silyl]oxy}-4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]butyl)-2-morpholin-4-yl-10H-phenothiazine 5,5-dioxide

: 1442372-01-1
4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 20 ℃; for 4.5h; Inert atmosphere;
DOI:10.1016/j.bmc.2013.04.034

Reference yield:

: 1387627-09-9
1-(2-chloro-10H-phenothiazin-10-yl)-4-(2-(4-methoxyphenyl)-2H-tetrazol-5-yl)butan-2-ol

: 1442372-01-1
4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 1H-imidazole / dichloromethane / 96 h / 0 - 20 °C / Inert atmosphere

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 - 20 °C

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 6 h / 0 - 20 °C

4: XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium t-butanolate / toluene / 1.5 h / 70 - 90 °C / Inert atmosphere

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 4.5 h / 0 - 20 °C / Inert atmosphere

With 1H-imidazole; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid; sodium t-butanolate; XPhos; In tetrahydrofuran; dichloromethane; toluene; 4: |Buchwald-Hartwig Coupling;
DOI:10.1016/j.bmc.2013.04.034

Reference yield:

: 1442371-84-7
10-(2-{[tert-butyl(diphenyl)silyl]oxy}-4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]butyl)-2-chloro-10H-phenothiazine

: 1442372-01-1
4-[2-(4-methoxyphenyl)-2H-tetrazol-5-yl]-1-(2-morpholin-4-yl-5,5-dioxido-10H-phenothiazin-10-yl)butan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 - 20 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 6 h / 0 - 20 °C

3: XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium t-butanolate / toluene / 1.5 h / 70 - 90 °C / Inert atmosphere

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 4.5 h / 0 - 20 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid; sodium t-butanolate; XPhos; In tetrahydrofuran; dichloromethane; toluene; 3: |Buchwald-Hartwig Coupling;
DOI:10.1016/j.bmc.2013.04.034