1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

Base Information

Chemical Name:1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol
CAS No.:1361215-54-4
Molecular Formula:C₁₈H₂₁F₃N₂O₄S₂
Molecular Weight:450.503
Hs Code.:

Synonyms:1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

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Chemical Property of 1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

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Technology Process of 1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

There total 6 articles about 1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol 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:

: 1361215-53-3
2-(4-((2R)-2-((benzyloxy)methyl)-4-(thiophen-2-ylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-2-propanol

: 1361215-54-4
1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

Guidance literature:: 2-(4-((2R)-2-((benzyloxy)methyl)-4-(thiophen-2-ylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-2-propanol; With boron trichloride; In dichloromethane; at 0 ℃; for 0.666667h;

With methanol; In dichloromethane;

Reference yield:

: 106-37-6
1.4-dibromobenzene

: 1361215-54-4
1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / diethyl ether; hexanes / 0.25 h / -78 °C

1.2: 0.5 h / -78 °C

2.1: sodium t-butanolate / ruphos; chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct / toluene / 12 h / 65 °C / sealed vessel; Inert atmosphere

3.1: boron trichloride / dichloromethane / 0.67 h / 0 °C

With n-butyllithium; boron trichloride; sodium t-butanolate; chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct; ruphos; In hexanes; diethyl ether; dichloromethane; toluene;

Reference yield:

: 1361215-52-2
(3R)-3-((benzyloxy)methyl)-1-(2-thiophenylsulfonyl)piperazine

: 1361215-54-4
1,1,1-trifluoro-2-(4-((2R)-2-(hydroxymethyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

Guidance literature:: Multi-step reaction with 2 steps

1: sodium t-butanolate / ruphos; chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct / toluene / 12 h / 65 °C / sealed vessel; Inert atmosphere

2: boron trichloride / dichloromethane / 0.67 h / 0 °C

With boron trichloride; sodium t-butanolate; chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct; ruphos; In dichloromethane; toluene;