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

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Chemical Name:2-(4-((2R)-2-((benzyloxy)methyl)-4-(thiophen-2-ylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-2-propanol
CAS No.:1361215-53-3
Molecular Formula:C₂₅H₂₇F₃N₂O₄S₂
Molecular Weight:540.628
Hs Code.:

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

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Chemical Property of 2-(4-((2R)-2-((benzyloxy)methyl)-4-(thiophen-2-ylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-2-propanol

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Technology Process of 2-(4-((2R)-2-((benzyloxy)methyl)-4-(thiophen-2-ylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-2-propanol

There total 5 articles about 2-(4-((2R)-2-((benzyloxy)methyl)-4-(thiophen-2-ylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-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:

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

: 122243-28-1
2‐(4‐bromophenyl)‐1,1,1‐trifluoropropan‐2‐ol

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

Guidance literature:: With 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 toluene; at 65 ℃; for 12h; sealed vessel; Inert atmosphere;

Reference yield:

: 106-37-6
1.4-dibromobenzene

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

Guidance literature:: Multi-step reaction with 2 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

With n-butyllithium; 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; toluene;

Reference yield:

: 23680-31-1
BOC-O-benzyl-L-serine

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

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 1 h

1.3: 16 h / 20 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 °C / Reflux

3.1: triethylamine / dichloromethane / 0.5 h / 0 °C

4.1: sodium t-butanolate / toluene / 0.08 h

4.2: 12 h / 65 °C / Sealed tube

With lithium aluminium tetrahydride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; sodium t-butanolate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene;