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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064139Generated: November 3, 2026

Hydrazine hydrate (1:1) → 1,1-Dimethylethyl 4-[(2-amino-4-fluoro-5-methylphenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/2064139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantTert-butyl 4-[(4-fluoro-5-methyl-2-nitrophenyl)amino]piperidine-1-carboxylateHCID 51072029—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product1,1-Dimethylethyl 4-[(2-amino-4-fluoro-5-methylphenyl)amino]-1-piperidinecarboxylateHCID 5985018392%

Reaction Conditions

Temperature45 °C

Reaction Steps

1,1-Dimethylethyl 4-[(4-fluoro-5-methyl-2-nitrophenyl)amino]-1-piperidinecarboxylate (D27) (0.96 mmol, 340 mg) in ethanol (20 mL) was treated under argon at room temperature with Raney Nickel (suspension, 50% in water, 0.5 mL) then dropwise with hydrazine hydrate (9.6 mmol, 10 eq) in ethanol over 15 min. The mixture was heated at 45° C. for 50 min. The Raney nickel was filtered off and washed with ethanol. The reaction mixture was concentrated under vacuum to give the title compound (0.88 mmol, 284 mg, 92% yield). M+H=324.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288412B2
Source datasetuspto-grants-2012_10
ORD IDord-824004b3439b4d94975c2c8858a6c710
Source noteuspto-grants-2012_10