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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363604Generated: October 30, 2026

Hydrochloric Acid → 1-(3-Aminopropyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine dihydrochloride

https://huagongshe.com/reaction/363604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidinyl]propyl]phthalimideHCID 15816943—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product1-(3-Aminopropyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine dihydrochlorideHCID 21960006—

Reaction Steps

A mixture of N-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propyl]phthalimide (8.5 g, 21 mmol), hydrazine monohydrate (1.5 g, 30 mmol) in methanol (60 ml) was heated at reflux for hours. At the end of the reaction, methanol was removed to leave a crude solid. To this was added water (60 ml), then the mixture was acidified with HCl to pH 1. The insolubles were filtered with the aid of a pad of Celite. The aqueous solution was basified with 50% NaOH, (pH 13), then extracted with dichloromethane. The combined dichloromethane solution was washed with brine, then dried to a colorless oil (4.5 g). The analytical sample (1.5 g) was prepared by treating the oil with HCl in ethanol at 0° C. The 1-(3-aminopropyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine dihydrochloride was obtained as white crystals, 2.03 g, m.p.=231°-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874435
Source datasetuspto-grants-1999_02
ORD IDord-1d718221126a4eb7bb05e5664a1aacd8
Source noteuspto-grants-1999_02