(Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

Base Information

Chemical Name:(Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid
CAS No.:114875-61-5
Molecular Formula:C₅₆H₄₄N₄O₆S
Molecular Weight:901.055
Hs Code.:

Synonyms:(Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

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Chemical Property of (Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

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Technology Process of (Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

There total 8 articles about (Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid 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: 85.0%

: 2-aminooxymethyl-1,5-bis-benzhydryloxy-1H-pyridin-4-one

: 68363-44-0
2-oxo-2-(2-(tritylamino)thiazol-4-yl)acetic acid

: 114875-61-5
(Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

Guidance literature:: In ethanol; dichloromethane; at 20 ℃; for 10h;

Reference yield:

: 59281-02-6
5-benzhydryloxy-2-(hydroxymethyl)-pyran-4-one

: 114875-61-5
(Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydroxylamine hydrochloride; sodium acetate trihydrate / ethanol; water / 18 h / 60 °C

2.1: potassium carbonate; sodium iodide / dimethyl sulfoxide / 17 h / 20 - 110 °C

3.1: triphenylphosphine; diethylazodicarboxylate / dimethyl sulfoxide; tetrahydrofuran / 1 h / 20 °C / Cooling with ice

3.2: 2 h / 75 °C

4.1: hydrazine hydrate / ethanol / 2 h / 75 °C

5.1: ethanol; dichloromethane / 10 h / 20 °C

With hydrazine hydrate; hydroxylamine hydrochloride; sodium acetate trihydrate; potassium carbonate; triphenylphosphine; sodium iodide; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide;

Reference yield:

: 1,5-bis(benzhydryloxy)-2-(hydroxymethyl)pyridin-4(1H)-one

: 114875-61-5
(Z)-2-(((1,5-bis(benzhydryloxy)-4-oxo-1,4-dihydropyridin-2-yl)methoxy)imino)-2-(2-(tritylamino)thiazol-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine; diethylazodicarboxylate / dimethyl sulfoxide; tetrahydrofuran / 1 h / 20 °C / Cooling with ice

1.2: 2 h / 75 °C

2.1: hydrazine hydrate / ethanol / 2 h / 75 °C

3.1: ethanol; dichloromethane / 10 h / 20 °C

With hydrazine hydrate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide;