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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042584Generated: November 2, 2026

Tert-butyl 4-hydroxypiperidine-1-carboxylate → HCID 59652002, compound

https://huagongshe.com/reaction/2042584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 59652048HCID 59652048—
SolventTolueneHCID 1140—
ProductHCID 59652002HCID 59652002—

Reaction Conditions

Temperature80 °C

Reaction Steps

To 6-(6-chloro-pyridin-3-yl)-2-methyl-2H-pyridazin-3-one (3 g, 13.6 mmol) in toluene (50 mL) was added 4-hydroxy-boc-piperidine (2.7 g, 13.6 mmol) and 1M KtOBu (16.3 mL, 16.3 mmol). After overnight stirring at 80° C., the reaction was concentrated, partitioned between dichloromethane/1N sodium carbonate, washed with water/brine, dried over sodium sulfate, and concentrated. The product was purified by column chromatography (99:1 dichloromethane:methanol) to obtain 2.7 g (51%); MS m/z 387 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586588B2
Source datasetuspto-grants-2013_11
ORD IDord-89dcc3702de94aa889a97933572e4340
Source noteuspto-grants-2013_11