methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

Base Information

Chemical Name:methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate
CAS No.:1445789-20-7
Molecular Formula:C₂₅H₂₆ClN₃O₄
Molecular Weight:467.952
Hs Code.:

Synonyms:methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

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Chemical Property of methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

Chemical Property:

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Technology Process of methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

There total 11 articles about methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate 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: 40.0%

: 1445790-46-4
methyl 3-amino-5-cyclopentylbenzoate

: 1445789-18-3
4,7-dichloro-6-ethoxyquinoline-3-carboxamide

: 1445789-20-7
methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

Guidance literature:: In ethanol; for 16h; Reflux;

Reference yield:

: 7-chloro-4-hydroxy-6-methoxyquinoline-3-carboxylic acid

: 1445789-20-7
methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate; water / 3 h / Reflux

2: ammonium hydroxide / tetrahydrofuran / 0 °C

3: boron tribromide / dichloromethane / 84 h / 40 °C / Inert atmosphere

4: potassium carbonate / N,N-dimethyl-formamide / 3 h / 70 °C / Sealed tube

5: ethanol / 16 h / Reflux

With ammonium hydroxide; water; boron tribromide; potassium carbonate; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: C₁₁H₇Cl₂NO₃

: 1445789-20-7
methyl 3-(3-carbamoyl-7-chloro-6-ethoxyquinolin-4-ylamino)-5-cyclopentylbenzoate

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium hydroxide / tetrahydrofuran / 0 °C

2: boron tribromide / dichloromethane / 84 h / 40 °C / Inert atmosphere

3: potassium carbonate / N,N-dimethyl-formamide / 3 h / 70 °C / Sealed tube

4: ethanol / 16 h / Reflux

With ammonium hydroxide; boron tribromide; potassium carbonate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;