1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

Base Information

Chemical Name:1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester
CAS No.:1393449-27-8
Molecular Formula:C₂₈H₄₀N₂O₃
Molecular Weight:452.637
Hs Code.:

Synonyms:1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

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Chemical Property of 1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

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Technology Process of 1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

There total 7 articles about 1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl 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: 66.0%

: 1126-09-6
4-carbethoxypiperidine

: 1266118-73-3
7-(trans-4-tert-butylcyclohexyloxy)isoquinoline-3-carbaldehyde

: 1393449-27-8
1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

Guidance literature:: 4-carbethoxypiperidine; 7-(trans-4-tert-butylcyclohexyloxy)isoquinoline-3-carbaldehyde; With triethylamine; In 1,2-dichloro-ethane; at 20 ℃; for 1h;

With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; for 2h;

Reference yield:

: 5071-96-5
3-METHOXYBENZYLAMINE

: 1393449-27-8
1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium sulfate; acetic acid / 1.5 h / 20 °C

1.2: 2.67 h

1.3: pH 7

2.1: trifluoroacetic acid / 55 °C / Inert atmosphere

3.1: air / copper(l) iodide / isopropyl alcohol / 54 h / 20 - 55 °C

4.1: boron tribromide / dichloromethane / 2.5 h / 20 °C

5.1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 20 °C

6.1: selenium(IV) oxide / diphenylether / 4 h / 200 °C / Sealed tube

7.1: triethylamine / 1,2-dichloro-ethane / 1 h / 20 °C

7.2: 2 h

With selenium(IV) oxide; di-isopropyl azodicarboxylate; boron tribromide; acetic acid; sodium sulfate; triethylamine; triphenylphosphine; trifluoroacetic acid; copper(l) iodide; In diphenylether; dichloromethane; 1,2-dichloro-ethane; isopropyl alcohol; toluene;

Reference yield:

: 83903-87-1
1,1-dimethoxy-N-(3-methoxybenzyl)propan-2-amine

: 1393449-27-8
1-[7-(trans-4-tert-butylcyclohexyloxy)isoquinolin-3-ylmethyl]piperidine-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: trifluoroacetic acid / 55 °C / Inert atmosphere

2.1: air / copper(l) iodide / isopropyl alcohol / 54 h / 20 - 55 °C

3.1: boron tribromide / dichloromethane / 2.5 h / 20 °C

4.1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 20 °C

5.1: selenium(IV) oxide / diphenylether / 4 h / 200 °C / Sealed tube

6.1: triethylamine / 1,2-dichloro-ethane / 1 h / 20 °C

6.2: 2 h

With selenium(IV) oxide; di-isopropyl azodicarboxylate; boron tribromide; triethylamine; triphenylphosphine; trifluoroacetic acid; copper(l) iodide; In diphenylether; dichloromethane; 1,2-dichloro-ethane; isopropyl alcohol; toluene;