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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363899Generated: October 31, 2026

Toluene → Vernakalant Hydrochloride

https://huagongshe.com/reaction/2363899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIsopropylamineHCID 6363—
ReactantRed-AlHCID 16684438—
ReactantHCID 178506527HCID 178506527—
ProductVernakalant HydrochlorideHCID 9930048—
ProductRed-AlHCID 16684438—

Reaction Steps

To a refluxing solution of Red-Al (65 wt % in toluene, 1.86 g, 1.80 mL, 6 mmol, Aldrich cat #19, 619-3) in toluene (2 mL) was added dropwise (over 5 min) a solution of crude (36) in toluene (3 mL). After the resultant solution was refluxed for 1 h, TLC analysis (EtOAc-hexanes, 2:1 v/v, +0.5% v/v iPrNH2) revealed the absence of (36) and the appearance of a new polar spot (reduction of (36) with Red-Al at room temperature provided a very complex mixture (HPLC) from which (19) could not be isolated). The cooled (0° C.) reaction mixture was cautiously quenched by addition of 6M aq NaOH (3 mL). After separation of the layers, the organic layer was dried over anhydrous MgSO4 and concentrated in vacuo to give (19) free base as an oil (195 mg, 37% yield). Alternatively, the reduction of (36) was performed using LiAlH4.THF2 1.0M in toluene (3 mL, 3 mmol, Aldrich cat #243949) at room temperature. After carefully quenching the reaction by successive addition of water (100 μl), 6M aq NaOH (100 μL) and water (300 μL), the free base of (19) (423 mg, 80% yield) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08692002B2
Source datasetuspto-grants-2014_04
ORD IDord-d6705040c7ca474bb873370261d24aa4
Source noteuspto-grants-2014_04