N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

Base Information

Chemical Name:N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide
CAS No.:1390635-82-1
Molecular Formula:C₂₆H₂₂FN₅O₂S
Molecular Weight:487.557
Hs Code.:

Synonyms:N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

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Chemical Property of N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

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Technology Process of N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

There total 5 articles about N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide 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: 76.0%

: 118887-70-0
2-azido-1-(4-fluoro-phenyl)-ethanone

: 309924-32-1
N'-(2-propynyl)-β-(10-phenothiazinyl)propionamide

: 1390635-82-1
N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

Guidance literature:: With copper(II) sulfate; sodium L-ascorbate; In methanol; water; acetonitrile; tert-butyl alcohol; at 50 ℃; for 24h;
DOI:10.1016/j.bmcl.2012.06.007

Reference yield:

: 1698-80-2
10H-phenothiazine-10-propanenitrile

: 1390635-82-1
N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

Guidance literature:: Multi-step reaction with 4 steps

1: water; sodium hydroxide / methanol / 15 h / Reflux

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 24 h / 20 °C

3: triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C

4: copper(II) sulfate; sodium L-ascorbate / methanol; water; acetonitrile; tert-butyl alcohol / 24 h / 50 °C

With water; copper(II) sulfate; sodium L-ascorbate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1016/j.bmcl.2012.06.007

Reference yield:

: 136832-74-1
2,5-dioxopyrrolidin-1-yl 3-(10H-phenothiazin-10-yl)propanoate N-hydroxysuccinimide ester

: 1390635-82-1
N-({1-[2-(4-fluorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-3-(10H-phenothiazin-10-yl)propanamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C

2: copper(II) sulfate; sodium L-ascorbate / methanol; water; acetonitrile; tert-butyl alcohol / 24 h / 50 °C

With copper(II) sulfate; sodium L-ascorbate; triethylamine; In methanol; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1016/j.bmcl.2012.06.007