(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

Base Information

Chemical Name:(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester
CAS No.:1361345-12-1
Molecular Formula:C₂₈H₃₀FN₅O₅S
Molecular Weight:567.641
Hs Code.:

(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

Synonyms:(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

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Chemical Property of (R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

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Technology Process of (R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

There total 4 articles about (R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-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:

: 64-17-5
ethanol

: 1361345-51-8
(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,5,6,7,8-hexahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carbonyl chloride

: 1361345-12-1
(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

Guidance literature:: With triethylamine; In dichloromethane; for 16h;

Reference yield:

: 1361345-27-8
(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-ylpyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalen-4a-carboxylic acid methyl ester

: 1361345-12-1
(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: water; lithium hydroxide / tetrahydrofuran / 16 h / 60 °C

2.1: oxalyl dichloride / dichloromethane / 0.5 h

2.2: 2 h

3.1: triethylamine / dichloromethane / 16 h

With oxalyl dichloride; water; triethylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane;

Reference yield:

: 6-(morpholin-4-yl)pyridine-3-sulfonyl chloride

: 1361345-12-1
(R)-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridine-3-sulfonyl)-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene-4a-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / 1,4-dioxane; methanol / 1 h / 20 °C

1.2: 1 h / 0 - 20 °C

2.1: water; lithium hydroxide / tetrahydrofuran / 16 h / 60 °C

3.1: oxalyl dichloride / dichloromethane / 0.5 h

3.2: 2 h

4.1: triethylamine / dichloromethane / 16 h

With hydrogenchloride; oxalyl dichloride; water; triethylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;