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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038815Generated: November 2, 2026

HCID 67130065, compound → HCID 67130064, compound

https://huagongshe.com/reaction/1038815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67130065HCID 67130065—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 67130064HCID 6713006499.4%

Reaction Steps

In one portion, 10% Pd/C (0.159 g, 1.491 mmol) was added to a mixture of benzyl 4-((tert-butoxycarbonylamino)methyl)-4-(cyclopropylmethyl)piperidine-1-carboxylate (0.60 g, 1.5 mmol, prepared using AF from benzyl 4-cyanopiperidine-1-carboxylate [Oakwood] with (bromomethyl)cyclopropane, AE, O with Boc2O) in MeOH (50 mL) at rt. The mixture was stirred under H2 at rt overnight. The mixture was filtered and concentrated in vacuo to provide tert-butyl (4-(cyclopropylmethyl)piperidin-4-yl)methylcarbamate (0.40 g, 95%): LC/MS (Table 2, Method i) Rt=1.59 min; MS m/z: 269 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551981B2
Source datasetuspto-grants-2013_10
ORD IDord-3dceb02a0ada45f394a027fe50b47a0e
Source noteuspto-grants-2013_10