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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25156Generated: October 26, 2026

Sodium Hydroxide → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]pyrrolo[1,2-c]pyrimidine-3-carboxamide Hydrochloride

https://huagongshe.com/reaction/25156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDiphenylphosphinic chlorideHCID 73910—
Reactant(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 12494972—
ReactantPyrrolo[1,2-c]pyrimidine-3-carboxylic acid hydrochlorideHCID 69607058—
SolventTetrahydrofuranHCID 8028—
ProductN-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]pyrrolo[1,2-c]pyrimidine-3-carboxamide HydrochlorideHCID 69773092100%

Reaction Steps

Pyrrolo[1,2-c]pyrimidine-3-carboxylic acid hydrochloride (0.33 g, 1.66 mmol) and TEA (2.0 mL, 14.35 mmol) are dissolved in 15 mL THF. Diphenylphosphinic chloride (0.47 g, 1.99 mmol) is added dropwise. After 1 h, (R)-(+)-3-aminoquinuclidine dihydrochloride is added and the reaction is allowed to stir at RT. After 1 day, 1N NaOH is added and the mixture is extracted with CHCl3. The combined organic layers are dried (MgSO4), filtered and concentrated. The residue is purified by chromatography (Biotage 40S, 90:9:1 CHCl3/MeOH/NH4OH) to afford 0.45 g (100%) of product. The hydrochloride salt is prepared and recrystallized from CH3CN/Et2O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858613B2
Source datasetuspto-grants-2005_02
ORD IDord-4bcf1dbee79d43acbf8b6721c5e60614
Source noteuspto-grants-2005_02