2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

Base Information

Chemical Name:2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate
CAS No.:1528759-97-8
Molecular Formula:C₄₄H₅₃N₇O₇
Molecular Weight:791.948
Hs Code.:

2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

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Chemical Property of 2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

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Technology Process of 2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

There total 6 articles about 2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate 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:

: 1528760-01-1
benzyl 4-[(2,2-dimethylpropanoyl)oxy]piperidine-1-carboxylate

: 1528759-97-8
2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen; palladium 10% on activated carbon / tetrahydrofuran

1.2: 12 h / 0 - 20 °C / Inert atmosphere

2.1: sodium azide / N,N-dimethyl-formamide / 5 h / Inert atmosphere

3.1: triethylamine; / dichloromethane

With sodium azide; palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.201200616

Reference yield:

: 90066-13-0
5-carboxytetraethylrhodamine

: 1528759-97-8
2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate; 1-hydroxy-7-aza-benzotriazole; 4-methyl-morpholine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

2: triethylamine; / dichloromethane

With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.201200616

Reference yield:

: 1528760-02-2
1-(chloroacetyl)piperidin-4-yl 2,2-dimethylpropanoate

: 1528759-97-8
2-[6-(diethylamino)-3-(diethyliminio)-3H-xanthen-9-yl]-5-({[1-(2-{4-[(2,2-dimethylpropanoyl)-oxy]piperidin-1-yl}-2-oxoethyl)-1H-1,2,3-triazol-4-yl]methyl}carbamoyl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium azide / N,N-dimethyl-formamide / 5 h / Inert atmosphere

2: triethylamine; / dichloromethane

With sodium azide; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.201200616