N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

Base Information

Chemical Name:N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide
CAS No.:1404097-83-1
Molecular Formula:C₂₂H₂₂F₄N₂O₄S
Molecular Weight:486.487
Hs Code.:

Synonyms:N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

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Technology Process of N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

There total 6 articles about N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide 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: 50.1%

: 1404097-60-4
C₂₁H₂₀F₄N₂O₂

: 124-63-0
methanesulfonyl chloride

: 1404097-83-1
N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 - 25 ℃;
DOI:10.1021/jm301164y

Reference yield:

: 73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester

: 1404097-83-1
N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 20 - 25 °C

2: dichloromethane / 3 h / 0 - 25 °C

3: potassium carbonate / ethanol; water / 25 - 80 °C

4: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

5: hydrogenchloride / water; acetone / 0.5 h

6: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; dmap; sodium tetrahydroborate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In methanol; ethanol; dichloromethane; water; acetone;
DOI:10.1021/jm301164y

Reference yield:

: C₁₃H₁₄F₄N₂O*C₂HF₃O₂

: 1404097-83-1
N-(1-(3-fluoro-4-(trifluoromethyl)benzoyl)piperidin-4-yl)-N-(4-formylbenzyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / ethanol; water / 25 - 80 °C

2: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

3: hydrogenchloride / water; acetone / 0.5 h

4: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; acetone;
DOI:10.1021/jm301164y