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

Base Information

Chemical Name:N-({1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-2-(10H-phenothiazin-10-yl)acetamide
CAS No.:1390635-92-3
Molecular Formula:C₂₅H₂₀ClN₅O₂S
Molecular Weight:489.985
Hs Code.:

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

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

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

There total 3 articles about N-({1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-2-(10H-phenothiazin-10-yl)acetamide 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: 65.0%

: 26086-60-2
2-azido-4'-chloroacetophenone

: 1390635-99-0
2-(10H-phenothiazin-10-yl)-N-prop-2-ynylacetamide

: 1390635-92-3
N-({1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-2-(10H-phenothiazin-10-yl)acetamide

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:

: 68825-29-6
ethyl 2-(10H-phenothiazin-10-yl)acetate

: 1390635-92-3
N-({1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-2-(10H-phenothiazin-10-yl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: water; sodium hydroxide / methanol; ethanol / 1 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; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1016/j.bmcl.2012.06.007

Reference yield:

: 92-84-2
10H-phenothiazine

: 1390635-92-3
N-({1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-1,2,3-triazol-4-yl}methyl)-2-(10H-phenothiazin-10-yl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / N,N-dimethyl-formamide / 12 h / 0 - 20 °C

2: water; sodium hydroxide / methanol; ethanol / 1 h / Reflux

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

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

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

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