2-[(Pyridin-4-yl)methyl]-1H-indole

Base Information

Chemical Name:2-[(Pyridin-4-yl)methyl]-1H-indole
CAS No.:38072-83-2
Molecular Formula:C14H12N2
Molecular Weight:208.263
Hs Code.:
DSSTox Substance ID:DTXSID70540504
Wikidata:Q82416539
Mol file:38072-83-2.mol

Synonyms:2-[(Pyridin-4-yl)methyl]-1H-indole;38072-83-2;SCHEMBL6988526;DTXSID70540504

Suppliers and Price of 2-[(Pyridin-4-yl)methyl]-1H-indole

Supply Marketing:

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

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Chemical Property of 2-[(Pyridin-4-yl)methyl]-1H-indole

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:208.100048391
Heavy Atom Count:16
Complexity:223

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C(N2)CC3=CC=NC=C3

Technology Process of 2-[(Pyridin-4-yl)methyl]-1H-indole

There total 2 articles about 2-[(Pyridin-4-yl)methyl]-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:

: 3469-06-5
benzocyclobutenone

: 38072-83-2
2-<(4-pyridyl)methyl>-1H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) phenyl lithium / 1.) ether, RT; 2.) ether

2: 70 percent / HN₃, cc H₂SO₄ / benzene

With tris-(2-chloro-ethyl)-amine; sulfuric acid; phenyllithium; In benzene;
DOI:10.1016/S0040-4020(01)96432-4

Reference yield:

: 3515-46-6
3-hydroxy-3-<(4-pyridyl)methyl>-1H-indol-2-one

: 5275-07-0
3-<(4-pyridyl)methyl>-1H-indole

: 38072-83-2
2-<(4-pyridyl)methyl>-1H-indole

Guidance literature:: With methanol; sodium tetrahydroborate; toluene-4-sulfonic acid; Yield given. Multistep reaction. Yields of byproduct given; 1) t-BuOH, reflux, 3 h, 2) benzene, reflux, 3 h;