(S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

Base Information

Chemical Name:(S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine
CAS No.:1352130-02-9
Molecular Formula:C₂₅H₂₃F₃N₄O₂
Molecular Weight:468.478
Hs Code.:

Synonyms:(S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

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Chemical Property of (S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

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Technology Process of (S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

There total 7 articles about (S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine 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: 84.6%

: 1352130-01-8
(S,E)-1-(2-(aminooxy)-1-(3,4,5-trifluorophenyl)ethyl)-3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene)piperidin-2-one

: 1352130-02-9
(S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

Guidance literature:: With phosphorus pentoxide; In ethanol; at 80 ℃;
DOI:10.1021/jm201407j

Reference yield:

: 1213556-08-1
(S)-2-amino-2-(3,4,5-trifluorophenyl)ethanol

: 1352130-02-9
(S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

Guidance literature:: Multi-step reaction with 5 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

2: sodium methylate / methanol

3: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0.5 h / -10 - 20 °C / Inert atmosphere

4: hydrazine hydrate / ethanol

5: phosphorus pentoxide / ethanol / 80 °C

With phosphorus pentoxide; sodium methylate; benzotriazol-1-ol; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; 3: Mitsunobu reaction;
DOI:10.1021/jm201407j

Reference yield:

: 1367361-09-8
C₁₆H₁₄F₃NO₃

: 1352130-02-9
(S,E)-9-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)-4-(3,4,5-trifluorophenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]oxadiazine

Guidance literature:: Multi-step reaction with 6 steps

1: 20 % Pd(OH)2/C; hydrogen / methanol; water / 1 h

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

3: sodium methylate / methanol

4: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0.5 h / -10 - 20 °C / Inert atmosphere

5: hydrazine hydrate / ethanol

6: phosphorus pentoxide / ethanol / 80 °C

With phosphorus pentoxide; 20 % Pd(OH)2/C; hydrogen; sodium methylate; benzotriazol-1-ol; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; 4: Mitsunobu reaction;
DOI:10.1021/jm201407j