((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone

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Chemical Name:((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone
CAS No.:1445590-49-7
Molecular Formula:C₂₄H₃₂BrN₃O₃
Molecular Weight:490.44
Hs Code.:

Synonyms:((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone

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Chemical Property of ((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone

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Technology Process of ((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone

There total 10 articles about ((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)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: 68.0%

: 1445591-28-5
(S)-benzyl 3-(tert-butoxymethyl) morpholine-4-carboxylate

: 1445591-92-3
(1R,2R)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentanecarboxylic acid

: 1445590-49-7
((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)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 0 - 20 ℃; for 2h;

Reference yield:

: 1655-07-8
ethyl 2-oxocyclohexane carboxylate

: 1445590-49-7
((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone

Guidance literature:: Multi-step reaction with 8 steps

1.1: bromine / chloroform / 0 - 20 °C

1.2: 6 h / 0 °C

1.3: pH 5

2.1: acetic anhydride / 20 h / Reflux

3.1: quinine / toluene; tetrachloromethane / 60 h / -65 °C

4.1: lithium diisopropyl amide / tetrahydrofuran / 4 h / -78 °C / Inert atmosphere

5.1: acetonitrile / 5 h / 20 °C / Inert atmosphere

6.1: ammonium acetate / toluene / 6 h / 100 °C / Sealed tube

7.1: hydrogenchloride / water / 2 h / 80 °C

8.1: 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 / 2 h / 0 - 20 °C

With hydrogenchloride; ammonium acetate; bromine; acetic anhydride; 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; chloroform; water; toluene; acetonitrile;

Reference yield:

: 1461-96-7
cis-1,2-cyclopentanedicarboxylic acid

: 1445590-49-7
((1,2-trans)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((S)-3-(tert-butoxymethyl)morpholino)methanone

Guidance literature:: Multi-step reaction with 7 steps

1: acetic anhydride / 20 h / Reflux

2: quinine / toluene; tetrachloromethane / 60 h / -65 °C

3: lithium diisopropyl amide / tetrahydrofuran / 4 h / -78 °C / Inert atmosphere

4: acetonitrile / 5 h / 20 °C / Inert atmosphere

5: ammonium acetate / toluene / 6 h / 100 °C / Sealed tube

6: hydrogenchloride / water / 2 h / 80 °C

7: 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 / 2 h / 0 - 20 °C

With hydrogenchloride; ammonium acetate; acetic anhydride; 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;