4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate

Base Information

Chemical Name:4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate
CAS No.:1076222-58-6
Molecular Formula:C₂HF₃O₂*C₂₃H₂₁N₃O₂S
Molecular Weight:517.529
Hs Code.:

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 4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate

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Technology Process of 4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate

There total 4 articles about 4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate 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:

: 943614-81-1
4-(2-amino-4-methyl-phenylsulfanyl)-phenol

: 1076222-58-6
4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 5.5 h / Heating / reflux

2: ethanol / 4 h / Heating / reflux

In ethanol;

Reference yield:

: 943614-99-1
4-[2-(7-chloro-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol

: 1076222-58-6
4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 4 h / Heating / reflux

In ethanol;

Reference yield:

: 91870-15-4
2,5-dichloro-1,8-naphthyridine

: 1076222-58-6
4-[2-(7-ethoxy-[1,8]naphthyridin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 5.5 h / Heating / reflux

2: ethanol / 4 h / Heating / reflux

In ethanol;