[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

Base Information

Chemical Name:[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol
CAS No.:693288-06-1
Molecular Formula:C₂₀H₃₀N₂O₃S
Molecular Weight:378.536
Hs Code.:

[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1<i>H</i>-pyrazol-3-yl]-methanol

Synonyms:[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

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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 [1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

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Technology Process of [1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

There total 8 articles about [1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol 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: 44.0%

: 693288-05-0
{1-[3-methyl-1-(2-methylpropyl)butyl]-5-(4-methylthiophenyl)pyrazol-3-yl}methanol

: 693288-06-1
[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

Guidance literature:: With oxone; In methanol; at 20 ℃;
DOI:10.1021/jm030276s

Reference yield:

: 108-83-8
diisobutyl ketone

: 693288-06-1
[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

Guidance literature:: Multi-step reaction with 6 steps

1: 100 percent / methanol / 20 °C

2: 48 percent / sodium cyanoborohydride; aq. acetic acid / 20 °C

3: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 20 °C

4: 51 percent / trifluoroacetic acid / methanol / 70 °C

5: 92 percent / LiAlH₄ / tetrahydrofuran / 20 °C

6: 44 percent / aq. Oxone(R) / methanol / 20 °C

With lithium aluminium tetrahydride; oxone; sodium cyanoborohydride; acetic acid; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm030276s

Reference yield:

: 1778-09-2
4-(Methylthio)acetophenone

: 693288-06-1
[1-(1-isobutyl-3-methyl-butyl)-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: 79 percent / sodium methoxide / toluene / 2 h / 20 °C

2: 51 percent / trifluoroacetic acid / methanol / 70 °C

3: 92 percent / LiAlH₄ / tetrahydrofuran / 20 °C

4: 44 percent / aq. Oxone(R) / methanol / 20 °C

With lithium aluminium tetrahydride; oxone; sodium methylate; trifluoroacetic acid; In tetrahydrofuran; methanol; toluene;
DOI:10.1021/jm030276s