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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564562Generated: October 26, 2026

Hydrochloric Acid → tert-Butyl 4-{[3'-(aminomethyl)biphenyl-3-yl]methyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/564562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-Dimethylethyl 4-[(3'-cyano-3-biphenylyl)methylidene]-1-piperidinecarboxylateHCID 67005869—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-Butyl 4-{[3'-(aminomethyl)biphenyl-3-yl]methyl}piperidine-1-carboxylateHCID 5781336095.3%

Reaction Steps

1,1-Dimethylethyl 4-[(3′-cyano-3-biphenylyl)methylidene]-1-piperidinecarboxylate (0.517 g, 1.381 mmol) in methanol (138 mL) was applied on H-Cube hydrogenation apparatus. This resultant mixture was run with Pd(OH)2 cartridge at 1 mL/min, with 1 atmosphere at 20° C. HCl (1.38 mL, 1 N) was then added. One portion was run one time with a Pd(OH)2 cartridge at 1 mL/min, 1 atmosphere at 20° C. Another portion was run with 1 run with a Pd(OH)2 cartridge at 1 mL/min with 50 atmosphere and 20° C. Both portions were combined for 1 run using a Pd(OH)2 cartridge, under conditions of 1 mL/min with 1 atmosphere at 20° C. The reaction mixture was concentrated to afford the title compound (0.5008 g, 87%). LC-MS m/z 381 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067408B2
Source datasetuspto-grants-2011_11
ORD IDord-b951cacabf9549a0a05f25d48bbdc000
Source noteuspto-grants-2011_11