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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972570Generated: November 2, 2026

Diisopropylamine → HCID 56932771, compound

https://huagongshe.com/reaction/1972570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPotassium CarbonateHCID 11430—
Reactant((2R)-4-(2-thiophenylsulfonyl)-1-(4-(2,2,2-trifluoro-1-hydroxy-1-methylethyl)phenyl)-2-piperazinyl)methyl methanesulfonateHCID 86670301—
SolventAcetonitrileHCID 6342—
ProductHCID 56932771HCID 5693277164.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

A 5-mL microwave vial was charged with ((2R)-4-(thiophen-2-ylsulfonyl)-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenyl)piperazin-2-yl)methyl methanesulfonate (0.200 g, 0.378 mmol, Intermediate B) diisopropylamine (0.077 g, 0.757 mmol), potassium carbonate (0.105 g, 0.757 mmol), in 3 mL of MeCN. The vial was sealed and heated in an Initiator microwave reactor (Biotage AB, Inc., Uppsala, Sweden) at 140° C. for 30 min. The reaction mixture was filtered and the filtrate was concentrated. The crude product was purified by column chromatography on silica gel (40 g of silica gel, 10 to 40% EtOAc in hexanes) to afford 2-(4-((2S)-2-((bis(1-methylethyl)amino)methyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-1,1,1-trifluoro-2-propanol (0.130 g) as

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-1aef3c760f8043bdb697cfb376948dd6
Source noteuspto-grants-2013_04