3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester
• CAS No.: 114495-24-8
• Molecular Formula: C₂₈H₃₁N₃O₃
• Molecular Weight: 457.572
• Mol file: 114495-24-8.mol

Synonyms:3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester

Chemical Property of 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester

There total 5 articles about 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester 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:

3-(2-bromoethyl)-1H-indole (3389-21-7) → 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester (114495-24-8)

Guidance literature:

Multi-step reaction with 4 steps

1: 99 percent / diethyl ether / 3.25 h / 90 °C

2: sodium borohydride / ethanol / 0 degC then 90 min at room temperature

3: 90 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 3 h

4: 1.) m-chloroperbenzoic acid, trifluoroacetic acid / 1.) CH₂Cl₂, 1 h, 0 degC then 15 min at -13 degC; 2.) CH₂Cl₂/water

With dmap; sodium tetrahydroborate; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In diethyl ether; ethanol; dichloromethane;

DOI:10.1016/S0040-4020(01)86795-8

Reference yield:

3-benzyloxypyridine (76509-17-6) → 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester (114495-24-8)

Guidance literature:

Multi-step reaction with 4 steps

1: 99 percent / diethyl ether / 3.25 h / 90 °C

2: sodium borohydride / ethanol / 0 degC then 90 min at room temperature

3: 90 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 3 h

4: 1.) m-chloroperbenzoic acid, trifluoroacetic acid / 1.) CH₂Cl₂, 1 h, 0 degC then 15 min at -13 degC; 2.) CH₂Cl₂/water

With dmap; sodium tetrahydroborate; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In diethyl ether; ethanol; dichloromethane;

DOI:10.1016/S0040-4020(01)86795-8

Reference yield:

3-[2-(5-Benzyloxy-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-1H-indole (76509-19-8) → 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester (114495-24-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 3 h

2: 1.) m-chloroperbenzoic acid, trifluoroacetic acid / 1.) CH₂Cl₂, 1 h, 0 degC then 15 min at -13 degC; 2.) CH₂Cl₂/water

With dmap; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In dichloromethane;

DOI:10.1016/S0040-4020(01)86795-8

upstream raw materials:

potassium cyanide

3-[2-(5-Benzyloxy-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester

3-(2-bromoethyl)-1H-indole

3-benzyloxypyridine

Downstream raw materials:

3-Benzyloxy-1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridine-2-carbonitrile

1-Benzyloxy-3,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine