5-bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole

Base Information

• Chemical Name: 5-bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole
• CAS No.: 116480-53-6
• Molecular Formula: C14H15BrN2
• Molecular Weight: 291.19
• European Community (EC) Number: 827-190-5
• ChEMBL ID: CHEMBL27227
• DSSTox Substance ID: DTXSID70566320
• Nikkaji Number: J570.978D
• Pharos Ligand ID: 3MPAFALMJYB4
• Wikidata: Q72448098
• Mol file: 116480-53-6.mol

Synonyms:116480-53-6;5-bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole;TCMDC-139098;5-bromo-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole;5-bromo-3-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indole;CHEMBL27227;5-Bromo-3-(1-methyl-1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indole;IRJNNZSKGXPISD-UHFFFAOYSA-N;1H-Indole, 5-bromo-3-(1,2,3,6-tetrahydro-1-methyl-4-pyridinyl)-;SCHEMBL1275594;DTXSID70566320;TQP0492;BDBM50209178;MFCD09833477;AKOS025404300;AS-40576;A803622;5-bromo-3-(1,2,3,6-tetrahydro-1-methyl4-pyridinyl)-1H-indole

Chemical Property of 5-bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole

Chemical Property:

• Melting Point: 266-268℃
• PSA: 19.03000
• LogP: 3.58720
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 290.04186
• Heavy Atom Count: 17
• Complexity: 315

Purity/Quality:

97% ^*data from raw suppliers

5-Bromo-3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 22

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1CCC(=CC1)C2=CNC3=C2C=C(C=C3)Br

Technology Process of 5-bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole

There total 4 articles about 5-bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole 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: 95.0%

1-Methyl-4-piperidone (1445-73-4) + 5-bromo-1H-indole (10075-50-0) → 5-bromo-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (116480-53-6)

Guidance literature:

With potassium hydroxide; In ethanol; for 7h; Reflux;

DOI:10.1021/op100018r

Reference yield: 76.0%

pyrrolidine (123-75-1) + 1-Methyl-4-piperidone (1445-73-4) + 5-bromo-1H-indole (10075-50-0) → 5-bromo-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (116480-53-6)

Guidance literature:

In ethanol;

Reference yield:

5-bromo-1H-indole (10075-50-0) + 4-fluoro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole + 1-methylpiperidin-2-one (931-20-4) → 5-bromo-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (116480-53-6)

Guidance literature:

upstream raw materials:

1-Methyl-4-piperidone

5-bromo-1H-indole

pyrrolidine

1-methylpiperidin-2-one

Downstream raw materials:

5-Bromo-3-(1-methyl-4-piperidinyl)-1H-indole

5-(4-Aminophenyl)-3-(1-Methylpiperidin-4-yl)-1H-Indole

5-(4-Acetylphenyl)-3-(1-Methylpiperidin-4-yl)-1H-Indole

5-(4-Acetamidophenyl)-3-(1-Methylpiperidin-4-yl)-1H-Indole