ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Base Information

Chemical Name:ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate
CAS No.:1428796-84-2
Molecular Formula:C₂₇H₂₇FN₂O₅
Molecular Weight:478.52
Hs Code.:

Synonyms:ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Suppliers and Price of ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

There total 10 articles about ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate 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:

: 90151-40-9
4-amino-3-methoxybenzaldehyde

: 1428796-84-2
ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1: n-Butyl nitrite; copper(I) bromide / acetonitrile / 18 h / 20 °C

2: ammonium acetate; acetic acid / 18 h / 80 °C

3: sodium tetrahydroborate; borane-THF / tetrahydrofuran / 18 h / 0 - 65 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C / Inert atmosphere

5: trichlorophosphate / toluene / 2 h / 110 °C

6: potassium carbonate; triethylamine / acetonitrile / 2 h / 100 °C

7: palladium diacetate; sodium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / toluene / 80 °C

8: palladium diacetate; caesium carbonate; triphenylphosphine / 1,4-dioxane / 21.25 h / 80 °C / Inert atmosphere; Sealed tube

With sodium tetrahydroborate; borane-THF; n-Butyl nitrite; ammonium acetate; palladium diacetate; sodium carbonate; potassium carbonate; caesium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; copper(I) bromide; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; toluene; acetonitrile;

Reference yield:

: 1121-86-4
1-Fluoro-3-iodobenzene

: 1428796-83-1
ethyl 8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

: 1428796-84-2
ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Guidance literature:: With palladium diacetate; caesium carbonate; triphenylphosphine; In 1,4-dioxane; at 80 ℃; for 21.25h; Inert atmosphere; Sealed tube;

Reference yield:

: 704-13-2
5-formyl-2-nitrophenol

: 1428796-84-2
ethyl 3-(3-fluorophenyl)-8-methoxy-9-(morpholine-4-carbonyl)-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 10 steps

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

2: iron; ammonium chloride / ethanol; water / 2 h / 78 °C

3: n-Butyl nitrite; copper(I) bromide / acetonitrile / 18 h / 20 °C

4: ammonium acetate; acetic acid / 18 h / 80 °C

5: sodium tetrahydroborate; borane-THF / tetrahydrofuran / 18 h / 0 - 65 °C / Inert atmosphere

6: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C / Inert atmosphere

7: trichlorophosphate / toluene / 2 h / 110 °C

8: potassium carbonate; triethylamine / acetonitrile / 2 h / 100 °C

9: palladium diacetate; sodium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / toluene / 80 °C

10: palladium diacetate; caesium carbonate; triphenylphosphine / 1,4-dioxane / 21.25 h / 80 °C / Inert atmosphere; Sealed tube

With sodium tetrahydroborate; borane-THF; n-Butyl nitrite; ammonium acetate; palladium diacetate; iron; sodium carbonate; potassium carbonate; ammonium chloride; caesium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; copper(I) bromide; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;