(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

Base Information

Chemical Name:(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene
CAS No.:1361344-79-7
Molecular Formula:C₂₇H₂₈F₃N₅O₄S
Molecular Weight:575.612
Hs Code.:

(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

Synonyms:(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

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Chemical Property of (R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

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Technology Process of (R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

There total 3 articles about (R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene 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:

: 1717-59-5
2,2-difluoro-2-(fluorosulfonyl)acetic acid

: 1361345-28-9
[(R)-1-(4-fluorophenyl)-6-[[6-(4-morpholinyl)-3-pyridinyl]sulfonyl]-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalen-4a-yl]methanol

: 1361344-79-7
(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

Guidance literature:: With copper(l) iodide; In acetonitrile; at 50 ℃; for 30h; Inert atmosphere;

Reference yield:

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

: 1361344-79-7
(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

Guidance literature:: Multi-step reaction with 3 steps

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

1.2: 1 h / 0 - 20 °C

2.1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / -78 °C / Inert atmosphere

3.1: copper(l) iodide / acetonitrile / 30 h / 50 °C / Inert atmosphere

With hydrogenchloride; copper(l) iodide; diisobutylaluminium hydride; In 1,4-dioxane; methanol; dichloromethane; toluene; acetonitrile;

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

: 1361344-79-7
(R)-4a-difluoromethoxymethyl-1-(4-fluorophenyl)-6-(6-morpholin-4-yl-pyridinyl-3-sulfonyl)-4,4a,5,67,8-1H-hexahydro-1,2,6-triazacyclopenta[b]naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / -78 °C / Inert atmosphere

2: copper(l) iodide / acetonitrile / 30 h / 50 °C / Inert atmosphere

With copper(l) iodide; diisobutylaluminium hydride; In dichloromethane; toluene; acetonitrile;