Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473514Generated: October 31, 2026

Hydrazine → Tert-butyl 4-(3-(5-aminopent-1-ynyl)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/473514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantTert-butyl 4-(3-(5-(1,3-dioxoisoindolin-2-yl)pent-1-ynyl)phenoxy)piperidine-1-carboxylateHCID 67202792—
SolventEthanolHCID 702—
ProductTert-butyl 4-(3-(5-aminopent-1-ynyl)phenoxy)piperidine-1-carboxylateHCID 67203672—

Reaction Steps

To a solution of tert-butyl 4-(3-(5-(1,3-dioxoisoindolin-2-yl)pent-1-ynyl)phenoxy)piperidine-1-carboxylate (10.65 g, 21.8 mmol) in ethanol (100 ml) was added hydrazine (2.1 g, 65.4 mmol). The resulting solution was heated under reflux for two hours, then cooled to room temperature, filtered and concentrated. The residue was dissolved in ethyl acetate (200 ml). The resulting solution was extracted with water twice, brine once, then dried over magnesium sulfate. The resulting solution was filtered and concentrated to yield tert-butyl 4-(3-(5-aminopent-1-ynyl)phenoxy)piperidine-1-carboxylate as a brown oil. MH+ 359.33

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633322B2
Source datasetuspto-grants-2014_01
ORD IDord-28b58956e10947dbbcbada693d609cdd
Source noteuspto-grants-2014_01