{2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:{2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester
CAS No.:748772-48-7
Molecular Formula:C₃₀H₄₃N₃O₄
Molecular Weight:509.689
Hs Code.:

Synonyms:{2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

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Chemical Property of {2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

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Technology Process of {2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

There total 10 articles about {2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic 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: 35.0%

: 74-88-4
methyl iodide

: 748772-46-5
[2-(2-isopropoxy-phenylamino)-ethyl]-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

: 748772-48-7
{2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

Guidance literature:: [2-(2-isopropoxy-phenylamino)-ethyl]-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester; With sodium hydride; In DMF (N,N-dimethyl-formamide); at 0 - 25 ℃; for 0.5h;

methyl iodide; In DMF (N,N-dimethyl-formamide); at 0 - 25 ℃; for 4h;

Reference yield:

: 38753-50-3
1-isopropoxy-2-nitrobenzene

: 748772-48-7
{2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium dithionite; water / tetrahydrofuran / 3 h / 25 - 55 °C

2.1: isopropyl alcohol / 24 h / 85 °C

2.2: 24 h / 85 °C

3.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 5.25 h / 25 °C

4.1: dichloromethane / 0.75 h / 25 °C

5.1: sodium hydride / DMF (N,N-dimethyl-formamide) / 0.5 h / 0 - 25 °C

5.2: 4 h / 0 - 25 °C

With sodium dithionite; water; sodium tris(acetoxy)borohydride; sodium hydride; In tetrahydrofuran; DMF (N,N-dimethyl-formamide); dichloromethane; 1,2-dichloro-ethane; isopropyl alcohol;

Reference yield:

: 619-21-6
m-formylphenyl benzoic acid

: 748772-48-7
{2-[(2-isopropoxy-phenyl)-methyl-amino]-ethyl}-[3-(piperidine-1-carbonyl)-benzyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / DMF (N,N-dimethyl-formamide) / 18.25 h / 25 °C

2.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 5.25 h / 25 °C

3.1: dichloromethane / 0.75 h / 25 °C

4.1: sodium hydride / DMF (N,N-dimethyl-formamide) / 0.5 h / 0 - 25 °C

4.2: 4 h / 0 - 25 °C

With sodium tris(acetoxy)borohydride; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In DMF (N,N-dimethyl-formamide); dichloromethane; 1,2-dichloro-ethane;