2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

Base Information

Chemical Name:2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate
CAS No.:1352948-49-2
Molecular Formula:C₃₇H₄₄N₆O₅
Molecular Weight:652.794
Hs Code.:

Synonyms:2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

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Chemical Property of 2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

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Technology Process of 2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

There total 7 articles about 2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)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:

: 509148-13-4
1-(3-iodopropyl)-1,3-dihydrobenzoimidazol-2-one

: 2-morpholino-2-oxoethyl 3-((4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate hydrochloride

: 1352948-49-2
2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 55 ℃; for 60h;

Reference yield:

: 1129-28-8
3-methoxycarbonylbenzyl bromide

: 1352948-49-2
2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 50 h / 60 °C

2: lithium hydroxide monohydrate / water; methanol / 18 h / 20 °C

3: dmap; dicyclohexyl-carbodiimide / dichloromethane / 18 h / 20 °C

4: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

5: potassium carbonate / N,N-dimethyl-formamide / 60 h / 55 °C

With hydrogenchloride; dmap; lithium hydroxide monohydrate; potassium carbonate; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1021-25-6
1-Phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

: 1352948-49-2
2-morpholinoethyl 3-((4-oxo-8-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 50 h / 60 °C

3: lithium hydroxide monohydrate / water; methanol / 18 h / 20 °C

4: dmap; dicyclohexyl-carbodiimide / dichloromethane / 18 h / 20 °C

5: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

6: potassium carbonate / N,N-dimethyl-formamide / 60 h / 55 °C

With hydrogenchloride; dmap; lithium hydroxide monohydrate; potassium carbonate; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;