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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615404Generated: October 30, 2026

HCID 76012106, compound → HCID 53328217, compound

https://huagongshe.com/reaction/1615404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 76012106HCID 76012106—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53328217HCID 53328217—

Reaction Steps

The 4-((1-methylpyrrol-2-yl)-carbonyl)-N-(1-(4-(3-morpholino-3-oxopropen-1-yl)-phenyl)-piperidin-4-yl)-1-piperazinecarboxamide (100 mg, 0.19 mmol) obtained in Example 11 was dissolved in THF (20 ml) and methanol (5 ml), and 10% Pd—C (39 mg) was added thereto, followed by stirring in a hydrogen atmosphere for 12 hours. After the insoluble material was filtered with Celite, the filtrate was evaporated under reduced pressure, thereby obtaining 4-((1-methylpyrrol-2-yl)-carbonyl)-N-(1-(4-(3-morpholino-3-oxopropyl)-phenyl)-piperidin-4-yl)-1-piperazinecarboxamide (84 mg, 84%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765750B2
Source datasetuspto-grants-2014_07
ORD IDord-80a42a2b681547d2b64d7ef9fc6985da
Source noteuspto-grants-2014_07