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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944703Generated: November 4, 2026

Acetic Acid → 2-(4-Cyclopropylpiperazin-1-yl)-5-pyrrolidin-1-ylmethylbenzooxazole

https://huagongshe.com/reaction/1944703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(4-Cyclopropylpiperazin-1-yl)benzooxazole-5-carboxaldehydeHCID 59588796—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-(4-Cyclopropylpiperazin-1-yl)-5-pyrrolidin-1-ylmethylbenzooxazoleHCID 2372893140%

Reaction Steps

To a solution of 2-(4-cyclopropylpiperazin-1-yl)benzooxazole-5-carboxaldehyde (400 mg, 1.48 mmol) and pyrrolidine (210 mg, 2.96 mmol) in CH3OH/THF (36 mL, 1:3) was added acetic acid (142 mg, 2.37 mmol), followed by NaCNBH3 (137 mg, 2.37 mmol). The mixture was heated at reflux for 12 h. The volatiles were removed and the residue was diluted with water (5 mL). The resulting mixture was extracted with CH2Cl2 (3×10 mL) and the combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by column chromatography on silica gel (elute: 2% dichloromethane in methanol) to give 193 mg (40%) of 2-(4-cyclopropylpiperazin-1-yl)-5-pyrrolidin-1-ylmethylbenzooxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394842B2
Source datasetuspto-grants-2013_03
ORD IDord-5a7ef58419cf4688b0600b10f419a3b0
Source noteuspto-grants-2013_03