2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one

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Chemical Name:2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one
CAS No.:84158-25-8
Molecular Formula:C₃₈H₂₉BrN₄O₃S
Molecular Weight:701.643
Hs Code.:

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Chemical Property of 2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one

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Technology Process of 2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one

There total 6 articles about 2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-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: 40.0%

: 106-49-0,12221-03-3
p-toluidine

: 84158-21-4
2-(4-Bromo-phenyl)-3-[10-(2-chloro-acetyl)-10H-phenothiazin-3-yl]-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3,5-dihydro-imidazol-4-one

: 84158-25-8
2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one

Guidance literature:: With triethylamine; at 170 ℃; for 1h;

Reference yield:

: 103205-37-4
(Z)-2-Amino-3-(4-methoxy-phenyl)-acrylic acid

: 84158-25-8
2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / acetic anhydride, sodium acetate

2: 85 percent / sodium acetate / acetic acid / 3 h / Heating; or ZnCl₂, 170-190 deg C, 1 h

3: 30 percent / S, I₂ / various solvent(s) / 2 h / 200 - 210 °C / Heating

4: 50 percent / toluene / 2 h / Heating

5: 40 percent / triethylamine / 1 h / 170 °C

With iodine; sodium acetate; acetic anhydride; triethylamine; In acetic acid; toluene;

Reference yield:

: 1122-91-4
4-bromo-benzaldehyde

: 84158-25-8
2-(4-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-[10-(2-p-tolylamino-acetyl)-10H-phenothiazin-3-yl]-3,5-dihydro-imidazol-4-one

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / acetic anhydride, sodium acetate

2: 85 percent / sodium acetate / acetic acid / 3 h / Heating; or ZnCl₂, 170-190 deg C, 1 h

3: 30 percent / S, I₂ / various solvent(s) / 2 h / 200 - 210 °C / Heating

4: 50 percent / toluene / 2 h / Heating

5: 40 percent / triethylamine / 1 h / 170 °C

With iodine; sodium acetate; acetic anhydride; triethylamine; In acetic acid; toluene;