Pyrrolo[2,1-a]isoquinoline-3-carboxylic acid, 5,6-dihydro-8,9-dimethoxy-2-[5-methoxy-2,4-bis(phenylmethoxy)phenyl] -1-[4-methoxy-3-(phenylmethoxy)phenyl]-7-(phenylmethoxy)-, ethyl ester

Base Information

Chemical Name:Pyrrolo[2,1-a]isoquinoline-3-carboxylic acid, 5,6-dihydro-8,9-dimethoxy-2-[5-methoxy-2,4-bis(phenylmethoxy)phenyl] -1-[4-methoxy-3-(phenylmethoxy)phenyl]-7-(phenylmethoxy)-, ethyl ester
CAS No.:919082-35-2
Molecular Formula:C59H55NO10
Molecular Weight:938.086
Hs Code.:

Pyrrolo[2,1-a]isoquinoline-3-carboxylic acid,
5,6-dihydro-8,9-dimethoxy-2-[5-methoxy-2,4-bis(phenylmethoxy)phenyl]
-1-[4-methoxy-3-(phenylmethoxy)phenyl]-7-(phenylmethoxy)-, ethyl ester

Synonyms:

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Chemical Property of Pyrrolo[2,1-a]isoquinoline-3-carboxylic acid, 5,6-dihydro-8,9-dimethoxy-2-[5-methoxy-2,4-bis(phenylmethoxy)phenyl] -1-[4-methoxy-3-(phenylmethoxy)phenyl]-7-(phenylmethoxy)-, ethyl ester

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MSDS Files:: SDS file from LookChem

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Technology Process of Pyrrolo[2,1-a]isoquinoline-3-carboxylic acid, 5,6-dihydro-8,9-dimethoxy-2-[5-methoxy-2,4-bis(phenylmethoxy)phenyl] -1-[4-methoxy-3-(phenylmethoxy)phenyl]-7-(phenylmethoxy)-, ethyl ester

There total 12 articles about Pyrrolo[2,1-a]isoquinoline-3-carboxylic acid, 5,6-dihydro-8,9-dimethoxy-2-[5-methoxy-2,4-bis(phenylmethoxy)phenyl] -1-[4-methoxy-3-(phenylmethoxy)phenyl]-7-(phenylmethoxy)-, ethyl ester 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: 62.0%

: 47811-27-8
5-benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-isoquinoline

: 1034028-91-5
(Z)-ethyl 2,4-bis(benzyloxy)-5-methoxy-α-nitrocinnamate

: 919082-35-2
ethyl 1-(3-benzyloxy-4-methoxyphenyl)-2-(2,4-dibenzyloxy-5-methoxyphenyl)-7-benzyloxy-8,9-dimethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate

Guidance literature:: With sodium hydrogencarbonate; In acetonitrile; for 18h; Heating;
DOI:10.1021/jo061810h

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 919082-35-2
ethyl 1-(3-benzyloxy-4-methoxyphenyl)-2-(2,4-dibenzyloxy-5-methoxyphenyl)-7-benzyloxy-8,9-dimethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

2: sodium hydrogencarbonate / acetonitrile / 18 h / Heating

With sodium hydrogencarbonate; In acetonitrile;
DOI:10.1021/jo061810h

Reference yield:

: 19283-70-6
3,4-dimethoxysalicylaldehyde

: 919082-35-2
ethyl 1-(3-benzyloxy-4-methoxyphenyl)-2-(2,4-dibenzyloxy-5-methoxyphenyl)-7-benzyloxy-8,9-dimethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / acetone / 6 h / Heating

2: acetic acid; ethylenediamine / 20 °C

3: lithium aluminium tetrahydride / tetrahydrofuran / 24 h / 20 °C

4: sodium carbonate / dichloromethane; water / 2 h / 20 °C

5: trichlorophosphate / N,N-dimethyl-formamide / 3 h / 20 °C

6: sodium hydrogencarbonate / acetonitrile / 18 h / Heating

With lithium aluminium tetrahydride; sodium hydrogencarbonate; sodium carbonate; potassium carbonate; acetic acid; ethylenediamine; trichlorophosphate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile; 2: Knoevenagel reaction / 5: Bischler-Napieralski reaction;
DOI:10.1021/jo061810h