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4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride

Base Information
  • Chemical Name:4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride
  • CAS No.:1260492-58-7
  • Molecular Formula:C24H22Cl2N4O2*ClH
  • Molecular Weight:505.831
  • Hs Code.:
4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride

Synonyms:4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride

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Chemical Property of 4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride
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Technology Process of 4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride

There total 11 articles about 4-(2,4-dichlorobenzyloxy)-1-(10-methyl-5,6,7,8,9,10-hexahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepin-2-yl)pyridin-2(1H)-one hydrochloride 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:
Guidance literature:
4-(2,4-dichlorobenzyloxy)pyridin-2(1H)-one; tert-butyl 2-bromo-10-methyl-7,8,9,10-tetrahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepine-6(5H)-carboxylate; With 8-quinolinol; caesium carbonate; copper(l) iodide; In dimethyl sulfoxide; at 135 ℃; for 18h; Inert atmosphere;
With hydrogenchloride; In diethyl ether; dichloromethane; at 25 ℃; for 24h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 2 steps
1.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / toluene / 18 h / 105 °C / Inert atmosphere
2.1: caesium carbonate; 8-quinolinol / copper(l) iodide / dimethyl sulfoxide / 18 h / 135 °C / Inert atmosphere
2.2: 24 h / 25 °C / Inert atmosphere
With 8-quinolinol; 1,10-Phenanthroline; caesium carbonate; copper(l) iodide; In dimethyl sulfoxide; toluene;
Guidance literature:
Multi-step reaction with 9 steps
1.1: hydrazine / 0.5 h / 70 °C
2.1: diethyl ether / 1 h / 20 °C
3.1: toluene-4-sulfonic acid / 0.42 h / 160 °C
4.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / water; tetrahydrofuran / 5 h
5.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere
6.1: hydroxylamine hydrochloride; sodium acetate / ethanol; water / 4 h / Reflux
7.1: diphenyl phosphoryl azide / 8 h / 100 °C
7.2: pH 7
8.1: borane-THF / tetrahydrofuran / 18 h / Reflux
8.2: Reflux
8.3: 18 h / 20 °C / Inert atmosphere
9.1: caesium carbonate; 8-quinolinol / copper(l) iodide / dimethyl sulfoxide / 18 h / 135 °C / Inert atmosphere
9.2: 24 h / 25 °C / Inert atmosphere
With 8-quinolinol; borane-THF; diphenyl phosphoryl azide; hydroxylamine hydrochloride; sodium acetate; caesium carbonate; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; hydrazine; copper(l) iodide; In tetrahydrofuran; diethyl ether; ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
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