(Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

Base Information

Chemical Name:(Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one
CAS No.:1050393-41-3
Molecular Formula:C₂₆H₂₆ClN₃O₃
Molecular Weight:463.964
Hs Code.:

Synonyms:(Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

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Chemical Property of (Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

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Technology Process of (Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

There total 9 articles about (Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one 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:

: 68766-96-1
ethyl (R)-2-pyrrolidone-5-carboxylate

: 1050393-41-3
(Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

Guidance literature:: Multi-step reaction with 10 steps

1.1: triethylamine / dmap / tetrahydrofuran / 5 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: tetrahydrofuran / 1 h / -40 °C

3.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C

4.1: triethylamine / N,N-dimethyl-formamide / 14 h / 20 °C

4.2: 0.33 h / 20 °C

5.1: lithium borohydride / tetrahydrofuran / 13.5 h / 0 - 20 °C

6.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.58 h / -78 °C

6.2: 0.5 h / -78 - 20 °C

7.1: tetrahydrofuran / 1 h / -78 °C

8.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C

9.1: 2 h / 120 °C

10.1: L-Selectride / tetrahydrofuran / 1 h / 0 °C

10.2: 0.33 h / 0 °C

With hydrogenchloride; lithium borohydride; oxalyl dichloride; L-Selectride; dimethyl sulfoxide; triethylamine; dmap; In tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 870837-18-6
3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde

: 1050393-36-6
(1S,6S,8aR)-6-(4-chlorophenyl)-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazine-3,4-dione

: 1050393-41-3
(Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

Guidance literature:: (1S,6S,8aR)-6-(4-chlorophenyl)-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazine-3,4-dione; With L-Selectride; In tetrahydrofuran; at 0 ℃; for 1h;

With sodium hydroxide; water; In tetrahydrofuran; at 0 ℃; for 0.333333h;

3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde; With dihydrogen peroxide; triphenylphosphine hydrobromide; triethylamine; more than 3 stages;

Reference yield:

: 1050393-32-2
(S)-1-[(2R,5S)-5-(4-chlorophenyl)pyrrolidine-2-yl]ethanol

: 1050393-41-3
(Z)-(1S,6S,8aR)-6-(4-chlorophenyl)-3-[3-methoxy-4-(4-methylimidazol-1-yl)benzylidene]-1-methyltetrahydropyrrolo[2,1-c][1,4]oxazin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: 2 h / 120 °C

2.1: L-Selectride / tetrahydrofuran / 1 h / 0 °C

2.2: 0.33 h / 0 °C

With L-Selectride; In tetrahydrofuran;