ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

Base Information

Chemical Name:ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate
CAS No.:1262881-08-2
Molecular Formula:C₂₆H₂₄N₂O₄
Molecular Weight:428.488
Hs Code.:

Synonyms:ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

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Chemical Property of ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

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Technology Process of ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

There total 3 articles about ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate 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:

: 1262881-06-0
2-phenyl-1H-indol-6-ylmethyl acetate

: 21908-10-1
ethyl 6-formyl-2-pyridinecarboxylate

: 1262881-08-2
ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

Guidance literature:: With triethylsilane; trifluoroacetic acid; In dichloromethane; at 20 ℃; for 6h; Cooling with ice;

Reference yield:

: 1262881-04-8
(2-phenyl-1H-indole-6-yl)methanol

: 1262881-08-2
ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 2 h / 20 °C

2: trifluoroacetic acid; triethylsilane / dichloromethane / 6 h / 20 °C / Cooling with ice

With pyridine; triethylsilane; trifluoroacetic acid; In dichloromethane;

Reference yield:

: 110073-83-1
2-phenyl-indole-6-carboxylic acid

: 1262881-08-2
ethyl 6-(6-acetoxymethyl-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 9.08 h / 20 - 50 °C / Cooling with ice

1.2: 20 °C

2.1: pyridine / dichloromethane / 2 h / 20 °C

3.1: trifluoroacetic acid; triethylsilane / dichloromethane / 6 h / 20 °C / Cooling with ice

With pyridine; triethylsilane; lithium aluminium tetrahydride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;