3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

Base Information

Chemical Name:3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine
CAS No.:796113-78-5
Molecular Formula:C₂₁H₂₅FN₄O₂
Molecular Weight:384.454
Hs Code.:

3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1<i>H</i>-pyrrolo[2,3-<i>b</i>]pyridine

Synonyms:3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

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Chemical Property of 3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

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Technology Process of 3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

There total 5 articles about 3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine 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:

: 4649-09-6
1H-pyrrolo[2,3-b]pyridin-3-carbaldehyde

: 796113-78-5
3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / NaBH₃CN; acetic acid / methanol / 18 h / 60 °C / pH 5

2: 65 percent / H₂SO₄ / methanol / 1 h / 60 °C

3: 64 percent / Et₃N / acetonitrile / 1 h / Heating

With sulfuric acid; sodium cyanoborohydride; acetic acid; triethylamine; In methanol; acetonitrile;
DOI:10.1016/j.bmc.2004.08.011

Reference yield:

: 345-29-9
4-fluorosalicylic acid

: 796113-78-5
3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / NaH / dimethylformamide / 14 h / 20 °C

2: 62 percent / LiAlH₄ / tetrahydrofuran / 14 h / 20 °C

3: 84 percent / Et₃N / CH₂Cl₂ / 0.5 h / 20 °C

4: 64 percent / Et₃N / acetonitrile / 1 h / Heating

With lithium aluminium tetrahydride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmc.2004.08.011

Reference yield:

: 625386-56-3
4-(1H-pyrrolo[2,3-b]pyridin-3-yl)piperazine-1-carboxaldehyde

: 796113-78-5
3-[4-(4-fluoro-2-methoxymethoxy-benzyl)-piperazin-1-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / H₂SO₄ / methanol / 1 h / 60 °C

2: 64 percent / Et₃N / acetonitrile / 1 h / Heating

With sulfuric acid; triethylamine; In methanol; acetonitrile;
DOI:10.1016/j.bmc.2004.08.011