1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

Base Information

Chemical Name:1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine
CAS No.:177945-99-2
Molecular Formula:C₂₈H₃₅N₇O
Molecular Weight:485.632
Hs Code.:

Synonyms:1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

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

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Chemical Property of 1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

There total 8 articles about 1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine 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: 64.0%

: 63630-08-0
N-[4-(2-aminoethyl)phenyl]acetamide

: 177947-84-1
1-{3-[5-(1,2,4-triazol-4-yl)-1H-indol-3-yl]propyl}piperidin-4-one

: 177945-99-2
1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

Guidance literature:: With sodium cyanoborohydride; acetic acid; In methanol; at 20 ℃; for 4h;
DOI:10.1021/jm9910021

Reference yield:

: 5382-16-1
4-HYDROXYPIPERIDINE

: 177945-99-2
1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

Guidance literature:: Multi-step reaction with 4 steps

1: 74 percent / K₂CO₃ / dimethylformamide / 3 h / 80 - 90 °C

2: 52 percent / aq. H₂SO₄ / 9 h / Heating

3: 69 percent / Et₃N; pyridine*SO₃ / dimethylsulfoxide / 0.92 h / 20 °C

4: 64 percent / gl.AcOH; NaCNBH₄ / methanol / 4 h / 20 °C

With sulfuric acid; sulfur trioxide pyridine complex; sodium cyanoborohydride; potassium carbonate; acetic acid; triethylamine; In methanol; dimethyl sulfoxide; N,N-dimethyl-formamide; 1: Alkylation / 2: Fisher indolization / 3: Oxidation / 4: reductive amination;
DOI:10.1021/jm9910021

Reference yield:

: 78643-42-2
5-bromopentanal dimethyl acetal

: 177945-99-2
1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]-4-[2-(4-acetylaminophenyl)ethylamino]piperidine

Guidance literature:: Multi-step reaction with 4 steps

1: 74 percent / K₂CO₃ / dimethylformamide / 3 h / 80 - 90 °C

2: 52 percent / aq. H₂SO₄ / 9 h / Heating

3: 69 percent / Et₃N; pyridine*SO₃ / dimethylsulfoxide / 0.92 h / 20 °C

4: 64 percent / gl.AcOH; NaCNBH₄ / methanol / 4 h / 20 °C

With sulfuric acid; sulfur trioxide pyridine complex; sodium cyanoborohydride; potassium carbonate; acetic acid; triethylamine; In methanol; dimethyl sulfoxide; N,N-dimethyl-formamide; 1: Alkylation / 2: Fisher indolization / 3: Oxidation / 4: reductive amination;
DOI:10.1021/jm9910021