1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

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Chemical Name:1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione
CAS No.:480434-40-0
Molecular Formula:C₃₃H₂₄N₄O₅S
Molecular Weight:588.643
Hs Code.:

Synonyms:1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

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Chemical Property of 1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

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Technology Process of 1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

There total 4 articles about 1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione 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: 82.0%

: 120-72-9
indole

: 480434-39-7
1-[(benzyloxy)methyl]-3-bromo-4-[1-(phenylsulphonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

: 480434-40-0
1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

Guidance literature:: indole; With ethylmagnesium bromide; In tetrahydrofuran; toluene; at 40 ℃; for 1h;

1-[(benzyloxy)methyl]-3-bromo-4-[1-(phenylsulphonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione; In tetrahydrofuran; toluene; at 40 ℃; for 15h; Further stages.;
DOI:10.1021/jm0210055

Reference yield:

: 271-63-6
7-Azaindole

: 480434-40-0
1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

Guidance literature:: Multi-step reaction with 3 steps

1.1: CH₃CH₂MgBr / tetrahydrofuran; toluene / 1.5 h / 20 °C

1.2: 57 percent / tetrahydrofuran; toluene; CH₂Cl₂ / 65 h / 40 °C

2.1: NaH / tetrahydrofuran / 1 h / 0 °C

2.2: 75 percent / tetrahydrofuran / 4 h / 20 °C

3.1: CH₃CH₂MgBr / tetrahydrofuran; toluene / 1 h / 40 °C

3.2: 82 percent / tetrahydrofuran; toluene / 15 h / 40 °C

With ethylmagnesium bromide; sodium hydride; In tetrahydrofuran; toluene;
DOI:10.1021/jm0210055

Reference yield:

: 102147-52-4
N-benzyloxymethyl-3,4-dibromomaleimide

: 480434-40-0
1-[(benzyloxy)methyl]-3-(1H-indol-3-yl)-4-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-1H-pyrrole-2,5-dione

Guidance literature:: Multi-step reaction with 3 steps

1.1: CH₃CH₂MgBr / tetrahydrofuran; toluene / 1.5 h / 20 °C

1.2: 57 percent / tetrahydrofuran; toluene; CH₂Cl₂ / 65 h / 40 °C

2.1: NaH / tetrahydrofuran / 1 h / 0 °C

2.2: 75 percent / tetrahydrofuran / 4 h / 20 °C

3.1: CH₃CH₂MgBr / tetrahydrofuran; toluene / 1 h / 40 °C

3.2: 82 percent / tetrahydrofuran; toluene / 15 h / 40 °C

With ethylmagnesium bromide; sodium hydride; In tetrahydrofuran; toluene;
DOI:10.1021/jm0210055