2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

Base Information

Chemical Name:2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate
CAS No.:1415043-86-5
Molecular Formula:C₂₇H₃₀FN₃O₅S
Molecular Weight:527.617
Hs Code.:

Synonyms:2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

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Chemical Property of 2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

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Technology Process of 2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

There total 8 articles about 2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate 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: 55.0%

: 108-01-0
2-(N,N-dimethylamino)ethanol

: 1415043-08-1
(3-{2-[(4-Fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetic acid

: 1415043-86-5
2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 5h;

Reference yield:

: 845267-78-9
tert-butyl 2,4-dioxopiperidine-1-carboxylate

: 1415043-86-5
2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / chloroform / 20 °C

2: sodium acetate / ethanol / 20 °C

3: acetic anhydride; hypophosphorous acid; water; hydrogen iodide / 96 h / 20 °C

4: dmap; dicyclohexyl-carbodiimide / dichloromethane / 5 h / 20 °C

With dmap; water; hydrogen iodide; sodium acetate; hypophosphorous acid; acetic anhydride; potassium carbonate; dicyclohexyl-carbodiimide; In ethanol; dichloromethane; chloroform;

Reference yield:

: [3-(2,2-dimethyl-4,6-dioxo-[1,3]-dioxan-5-yl)-3-oxo-propyl]-carbamic acid tert-butyl ester

: 1415043-86-5
2-(Dimethylamino)ethyl (3-{2-[(4-fluorophenyl)sulfonyl]benzyl}-2-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: ethyl acetate / 2.5 h / Reflux

2: potassium carbonate / chloroform / 20 °C

3: sodium acetate / ethanol / 20 °C

4: acetic anhydride; hypophosphorous acid; water; hydrogen iodide / 96 h / 20 °C

5: dmap; dicyclohexyl-carbodiimide / dichloromethane / 5 h / 20 °C

With dmap; water; hydrogen iodide; sodium acetate; hypophosphorous acid; acetic anhydride; potassium carbonate; dicyclohexyl-carbodiimide; In ethanol; dichloromethane; chloroform; ethyl acetate;