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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298370Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-(3-chlorophenyl)-1,3-oxazole-2-carboxamide 4-methylbenzenesulfonate

https://huagongshe.com/reaction/2298370

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant(3R)-1-Azabicyclo(2.2.2)octan-3-amineHCID 719215—
ReactantEthyl 5-(3-chlorophenyl)oxazole-2-carboxylateHCID 22350710—
SolventEthanolHCID 702—
ProductN-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-(3-chlorophenyl)-1,3-oxazole-2-carboxamide 4-methylbenzenesulfonateHCID 8658488370.9%

Reaction Steps

A mixture of the product from Step 79c (0.419 g, 1.66 mmol, 1.0 eq), (R)-(+)-3-aminoquinuclidine (0.221 g, 1.75 mmol, 1.05 eq) and EtOH (4.0 mL) is heated under reflux. After 64 h, the mixture is cooled and the contents are filtered through glass wool into p-toluenesulfonic acid monohydrate (0.315 g, 1.65 mmol, 1.0 eq). The resulting solid is filtered and dried in vacuity to afford the title compound (0.59 g, 65%). HRMS (FAB) calculated for C17H18ClN3O2+H1 332.1165, found 332.1180.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492385B2
Source datasetuspto-grants-2002_12
ORD IDord-850d867653b34a6798c6a743fcabbdb5
Source noteuspto-grants-2002_12