N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

Base Information

Chemical Name:N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide
CAS No.:118297-41-9
Molecular Formula:C₁₈H₂₁ClF₂N₂O₃
Molecular Weight:386.826
Hs Code.:

Synonyms:N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

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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 N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

Chemical Property:

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Technology Process of N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

There total 6 articles about N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide 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:

: 28177-48-2
2,6-difluorophenol

: 118297-41-9
N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: trifluoroacetic acid / Heating

2: K₂CO₃, NaI / dimethylformamide / 1.5 h / 100 °C

3: aq. AgNO₃, aq. KOH / ethanol / 0.83 h

4: SOCl₂ / 18 h / Ambient temperature

5: Et₃N / CHCl₃ / 18 h / Ambient temperature

With potassium hydroxide; thionyl chloride; potassium carbonate; silver nitrate; triethylamine; trifluoroacetic acid; sodium iodide; In ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm00122a027

Reference yield:

: 98033-85-3
5-(5-bromopentyl)-3-methylisoxazole

: 118297-41-9
N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: K₂CO₃, NaI / dimethylformamide / 1.5 h / 100 °C

2: aq. AgNO₃, aq. KOH / ethanol / 0.83 h

3: SOCl₂ / 18 h / Ambient temperature

4: Et₃N / CHCl₃ / 18 h / Ambient temperature

With potassium hydroxide; thionyl chloride; potassium carbonate; silver nitrate; triethylamine; sodium iodide; In ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm00122a027

Reference yield:

: 118276-06-5
3,5-difluoro-4-hydroxybenzaldehyde

: 118297-41-9
N-(2-Chloro-ethyl)-3,5-difluoro-4-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: K₂CO₃, NaI / dimethylformamide / 1.5 h / 100 °C

2: aq. AgNO₃, aq. KOH / ethanol / 0.83 h

3: SOCl₂ / 18 h / Ambient temperature

4: Et₃N / CHCl₃ / 18 h / Ambient temperature

With potassium hydroxide; thionyl chloride; potassium carbonate; silver nitrate; triethylamine; sodium iodide; In ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm00122a027