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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242782Generated: October 31, 2026

HCID 68157732, compound → HCID 68157390, compound

https://huagongshe.com/reaction/242782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68157732HCID 68157732—
CatalystPalladiumHCID 23938—
ProductHCID 68157390HCID 6815739091.1%

Reaction Steps

To a nitrogen purged solution of 4-[2-((S)-1-benzyloxycarbonylaminoethyl)benzoimidazol-1-yl]piperidine-1-carboxylic acid tertbutyl ester (308 mg, 0.644 mmol) in IMS (10 mL) was added 10% Pd/C (32 mg) and the reaction mixture was stirred at RT under a hydrogen atmosphere for 2 h. Additional quantities of 10% Pd/C were subsequently added (41 mg after 2 h and 33 mg after 4 h) and the reaction mixture was stirred at RT under a hydrogen atmosphere for 17 h. The suspension was filtered through a PTFE frit and washed with additional IMS. The filtrate was concentrated in vacuo affording 4-[2-((S)-1-Aminoethyl)benzoimidazol-1-yl]piperidine-1-carboxylic acid tertbutyl ester as a pale yellow oil (202 mg). LCMS: RT 2.34 min [M+H]+ 345.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-5f4ceb95a347465c85602f81212b7b61
Source noteuspto-grants-2014_02