methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

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Chemical Name:methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester
CAS No.:228259-15-2
Molecular Formula:C₁₇H₁₅F₃N₂O₅S
Molecular Weight:416.378
Hs Code.:

Synonyms:methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

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Chemical Property of methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

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Technology Process of methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

There total 6 articles about methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester 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:

: 326-90-9
4,4,4-trifluoro-1-(2-furanyl)-1,3-butanedione

: 228259-15-2
methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: AcOH / 4 h / 100 °C

2: N-methylmorpholine / tetrahydrofuran / 0.5 h / 0 °C

3: 1.5 g / NaBH₄ / tetrahydrofuran; H₂O

4: Et₃N / CHCl₃ / 4 h / cooling

With 4-methyl-morpholine; sodium tetrahydroborate; acetic acid; triethylamine; In tetrahydrofuran; chloroform; water;
DOI:10.1021/jm030212h

Reference yield:

: 6705-03-9
2-Amino-5-methoxybenzoic acid

: 228259-15-2
methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: HCl; NaNO₂ / H₂O / 0.5 h / 0 °C

1.2: SnCl₂*2H₂O; HCl / H₂O / 3 h / 0 - 20 °C

2.1: AcOH / 4 h / 100 °C

3.1: N-methylmorpholine / tetrahydrofuran / 0.5 h / 0 °C

4.1: 1.5 g / NaBH₄ / tetrahydrofuran; H₂O

5.1: Et₃N / CHCl₃ / 4 h / cooling

With 4-methyl-morpholine; hydrogenchloride; sodium tetrahydroborate; acetic acid; triethylamine; sodium nitrite; In tetrahydrofuran; chloroform; water;
DOI:10.1021/jm030212h

Reference yield:

: 228259-02-7
2-carboxy-4-methoxyphenylhydrazine

: 228259-15-2
methanesulfonic acid 2-(5-furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-5-methoxy-benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: AcOH / 4 h / 100 °C

2: N-methylmorpholine / tetrahydrofuran / 0.5 h / 0 °C

3: 1.5 g / NaBH₄ / tetrahydrofuran; H₂O

4: Et₃N / CHCl₃ / 4 h / cooling

With 4-methyl-morpholine; sodium tetrahydroborate; acetic acid; triethylamine; In tetrahydrofuran; chloroform; water;
DOI:10.1021/jm030212h