((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

Base Information

Chemical Name:((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone
CAS No.:1445590-34-0
Molecular Formula:C₁₉H₂₂BrN₃O₂
Molecular Weight:404.307
Hs Code.:

Synonyms:((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

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Chemical Property of ((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

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Technology Process of ((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

There total 13 articles about ((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone 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: 76.0%

: 953780-78-4,192661-47-5
(3R)-3-methylmorpholine hydrochloride

: 1445590-33-9
(1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutanecarboxylic acid

: 1445590-34-0
((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; at 20 ℃; Inert atmosphere;

Reference yield: 46.0%

: (1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutanecarboxylic acid hydrochloride

: 74572-04-6
(3R)-3-methylmorpholine

: 1445590-34-0
((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; at 20 ℃;

Reference yield:

: 4462-96-8
3-oxabicyclo[3.2.0]heptane-2,4-dione

: 1445590-34-0
((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclobutyl)((R)-3-methylmorpholino)methanone

Guidance literature:: Multi-step reaction with 6 steps

1: quinine / toluene; tetrachloromethane / 72 h / -50 °C

2: lithium diisopropyl amide / tetrahydrofuran / 1.5 h / -70 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 4 h / 20 °C

4: ammonium acetate / 2.5 h / 150 - 160 °C / Dean-Stark

5: hydrogenchloride / water / 3 h / 80 °C

6: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 20 °C

With hydrogenchloride; ammonium acetate; quinine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium diisopropyl amide; In tetrahydrofuran; tetrachloromethane; dichloromethane; water; toluene; acetonitrile;