(R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

Base Information

Chemical Name:(R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide
CAS No.:1418292-71-3
Molecular Formula:C₁₇H₂₀F₄N₄O₂
Molecular Weight:388.365
Hs Code.:

Synonyms:(R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

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Chemical Property of (R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

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Technology Process of (R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

There total 3 articles about (R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide 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:

: 1418293-47-6
2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid

: 486414-51-1,773045-76-4
(R)-3,N¹,N¹-trimethyl-butane-1,2-diamine

: 1418292-71-3
(R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

Guidance literature:: With 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 1418293-46-5
2-fluoro-4-(N-hydroxycarbamimidoyl)-benzoic acid

: 1418292-71-3
(R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 4.5 h

2: N-ethyl-N,N-diisopropylamine; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate / dichloromethane / 20 °C

With 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 164149-28-4
4-cyano-2-fluorobenzoic acid

: 1418292-71-3
(R)-N-(1-(dimethylamino)-3-methylbutan-2-yl)-2-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate; hydroxylamine hydrochloride; 8-quinolinol / ethanol; water / 4 h / Reflux

1.2: pH 3

2.1: tetrahydrofuran / 4.5 h

3.1: N-ethyl-N,N-diisopropylamine; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate / dichloromethane / 20 °C

With 8-quinolinol; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; hydroxylamine hydrochloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; water;