3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

Base Information

Chemical Name:3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride
CAS No.:115892-30-3
Molecular Formula:C₂₂H₂₇N₃O₂*ClH
Molecular Weight:401.936
Hs Code.:

Synonyms:3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

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Technology Process of 3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

There total 5 articles about 3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-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:

Reference yield: 47.0%

: 106536-45-2
2-bromo-N,N-dimethylethan-1-amine hydrochloride

: 89109-20-6
3-(n-butyl)-4-hydroxy-1-phenyl-1,8-naphthyridine-2(1H)-one

: 115892-30-3
3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

Guidance literature:: With potassium carbonate; In acetone; Heating; 1.) 0.5 h, 2.) 24 h;
DOI:10.1021/jm00119a010

Reference yield:

: 40134-18-7
methyl 2-chloropyridine-3-carboxylate

: 115892-30-3
3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent

2: 80 percent / potassium tert-butoxide / 1.) 0.25 h, 2.) heating, 4 h

3: 47 percent / 1.) potassium carbonate / acetone / Heating; 1.) 0.5 h, 2.) 24 h

With potassium tert-butylate; potassium carbonate; In acetone;
DOI:10.1021/jm00119a010

Reference yield:

: 51269-84-2
methyl 2-phenylamino-nicotinate

: 115892-30-3
3-Butyl-4-(2-dimethylamino-ethoxy)-1-phenyl-1H-[1,8]naphthyridin-2-one; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / potassium tert-butoxide / 1.) 0.25 h, 2.) heating, 4 h

2: 47 percent / 1.) potassium carbonate / acetone / Heating; 1.) 0.5 h, 2.) 24 h

With potassium tert-butylate; potassium carbonate; In acetone;
DOI:10.1021/jm00119a010