2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

Base Information

Chemical Name:2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide
CAS No.:187156-04-3
Molecular Formula:C₂₀H₁₈ClN₃O
Molecular Weight:351.835
Hs Code.:

Synonyms:2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

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Chemical Property of 2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

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Technology Process of 2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

There total 1 articles about 2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide 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: 70.0%

: 3612-20-2
1-phenylmethyl-4-piperidone

: 17630-76-1
5-chloroindole 2,3-dione

: 187156-04-3
2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

Guidance literature:: With ammonia; In ethylene glycol; at 150 - 160 ℃; for 1h;
DOI:10.1002/jhet.5570330642

Reference yield: 62.0%

: 67-56-1
methanol

: 187156-04-3
2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

: 187156-22-5
2-benzyl-8-chloro-10-methoxycarbonylamino-1,2,3,4-tetrahydrobenzo[b][1,6]naphthyridine

Guidance literature:: With bromine; sodium methylate; for 0.333333h; Heating;
DOI:10.1002/jhet.5570330642

Reference yield:

: 187156-04-3
2-Benzyl-8-chloro-1,2,3,4-tetrahydro-benzo[b][1,6]naphthyridine-10-carboxylic acid amide

: 10-amino-2-benzyl-8-chloro-1,2,3,4-tetrahydrobenzo[b][1,6]naphthyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / NaOMe, Br₂ / 0.33 h / Heating

2: 72 percent / 20percent aq. KOH / ethanol / 4 h / Heating

With potassium hydroxide; bromine; sodium methylate; In ethanol;
DOI:10.1002/jhet.5570330642