3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

Base Information

Chemical Name:3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide
CAS No.:1401461-20-8
Molecular Formula:C₂₈H₂₁N₇O₄S₂
Molecular Weight:583.651
Hs Code.:

Synonyms:3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

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Chemical Property of 3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

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Technology Process of 3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

There total 6 articles about 3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide 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: 19.5%

: 203268-83-1,32058-82-5
5-(4-aminophenyl)-1,3,4-oxadiazole-2-thiol

: 1401461-05-9
3-[7-(3,4-dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-benzoic acid

: 1401461-20-8
3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 40h;

Reference yield:

: 6315-89-5
3,4-dimethoxyaniline

: 1401461-20-8
3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 24 h / 20 °C

2.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 20 - 100 °C / Inert atmosphere

3.1: sodium hydroxide; water / tetrahydrofuran; methanol / 16 h / 20 °C

3.2: pH 3

4.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 40 h / 20 °C

With dmap; water; sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1401461-83-3
(5-chlorothiazolo[5,4-d]pyrimidin-7-yl)-(3,4-dimethoxyphenyl)amine

: 1401461-20-8
3-[7-(3,4-Dimethoxy-phenylamino)-thiazolo[5,4-d]pyrimidin-5-yl]-N-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 20 - 100 °C / Inert atmosphere

2.1: sodium hydroxide; water / tetrahydrofuran; methanol / 16 h / 20 °C

2.2: pH 3

3.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 40 h / 20 °C

With dmap; water; sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;