3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine

Base Information

Chemical Name:3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine
CAS No.:131248-92-5
Molecular Formula:C₂₁H₁₇ClN₂OS
Molecular Weight:380.898
Hs Code.:

3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<c><1,8>naphthyridine

Synonyms:

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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-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine

Chemical Property:

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Technology Process of 3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine

There total 3 articles about 3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine 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: 75.0%

: 131248-86-7
3-chloro-1-methyl-6-(p-methylphenoxy)benzo<1,8>naphthyridine

: 106-54-7
p-Chlorothiophenol

: 131248-92-5
3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine

Guidance literature:: In ethanol; for 2.25h; Heating;
DOI:10.1071/CH9901469

Reference yield:

: 106051-96-1
1-(p-methylphenoxy)isoquinoline-3-amine

: 131248-92-5
3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / acetic acid / 1.) 150 - 160 deg C, 1 h, 2.) reflux, 2 h

2: 67 percent / phosphoryl chloride / 0.33 h / Heating

3: 75 percent / ethanol / 2.25 h / Heating

With acetic acid; trichlorophosphate; In ethanol;
DOI:10.1071/CH9901469

Reference yield:

: 131248-84-5
1-methyl-6-(p-methylphenoxy)benzo<1,8>naphthyridin-3(4H)-one

: 131248-92-5
3-(p-chlorophenylthio)-1-methyl-6-ethoxybenzo<1,8>naphthyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / phosphoryl chloride / 0.33 h / Heating

2: 75 percent / ethanol / 2.25 h / Heating

With trichlorophosphate; In ethanol;
DOI:10.1071/CH9901469