dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

Base Information

Chemical Name:dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate
CAS No.:217302-97-1
Molecular Formula:C₃₆H₃₁NO₆
Molecular Weight:573.645
Hs Code.:

Synonyms:dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

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Chemical Property of dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

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Technology Process of dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

There total 8 articles about dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate 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:

: 762-42-5
dimethyl acetylenedicarboxylate

: 84-58-2
2,3-dicyano-5,6-dichloro-p-benzoquinone

: 217302-95-9
6-benzyloxy-2-(4-benzyloxyphenyl)-1-ethylindolizine

: 217302-97-1
dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

Guidance literature:: In toluene;

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 217302-97-1
dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: Na

2.1: aq. H₂SO₄ / 18 h / Heating

3.1: Pd/C / ethanol

4.1: NaNO₂; aq. HCl / 0.5 h / 0 °C

4.2: H₂O / 2 h / 70 °C

5.1: NaH / tetrahydrofuran / 0 °C

5.2: dimethylsulfoxide / 3 h / 25 °C

6.1: acetone / Heating

6.2: aq. NaHCO₃ / Heating

7.1: toluene / 0 °C

7.2: DDQ / Heating

With hydrogenchloride; sulfuric acid; sodium; sodium hydride; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetone; toluene; 1.1: Alkylation / 2.1: Hydrolysis / 3.1: Reduction / 4.1: Diazotization / 4.2: hydroxylation / 5.1: Metallation / 5.2: Alkylation / 6.1: quaternization / 6.2: Cyclization / 7.1: Cycloaddition / 7.2: Oxidation;
DOI:10.1016/S0960-894X(00)00474-1

Reference yield:

: 217302-90-4
5-nitro-2-propylpyridine

: 217302-97-1
dimethyl 7-benzyloxy-3-(4-benzyloxyphenyl)-4-ethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: Pd/C / ethanol

2.1: NaNO₂; aq. HCl / 0.5 h / 0 °C

2.2: H₂O / 2 h / 70 °C

3.1: NaH / tetrahydrofuran / 0 °C

3.2: dimethylsulfoxide / 3 h / 25 °C

4.1: acetone / Heating

4.2: aq. NaHCO₃ / Heating

5.1: toluene / 0 °C

5.2: DDQ / Heating

With hydrogenchloride; sodium hydride; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetone; toluene; 1.1: Reduction / 2.1: Diazotization / 2.2: hydroxylation / 3.1: Metallation / 3.2: Alkylation / 4.1: quaternization / 4.2: Cyclization / 5.1: Cycloaddition / 5.2: Oxidation;
DOI:10.1016/S0960-894X(00)00474-1