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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366478Generated: October 29, 2026

HCID 86636953, compound → HCID 58000758, compound

https://huagongshe.com/reaction/1366478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86636953HCID 86636953—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 58000758HCID 5800075862.7%

Reaction Steps

To a solution of [(2R)-2-(cyclopentylmethyl)-3-(2-{6-[(2R)-2,4-dimethyl-1-piperazinyl]-5-fluoro-2-methyl-4-pyrimidinyl}hydrazino)-3-oxopropyl][(phenylmethyl)oxy]formamide (15.60 g, 28.8 mmol) in methanol (115 mL) was added Pd/C (50% water, 3.1 g). The mixture was hydrogenated under balloon pressure for 2 h, and then filtered through a glass fiber filter. The solution was then concentrated in vacuo and azeotroped with EtOAc (100 mL). The resulting solid was triturated with 70% EtOAc in hexanes, and collected by vacuum filtration. The supernatant was concentrated in vacuo and crystallized from EtOAc-hexanes, and the solid was combined with the first crop of material. The combined solid was dried overnight under high vacuum to give [(2R)-2-(cyclopentylmethyl)-3-(2-{6-[(2R)-2,4-dimethyl-1-piperazinyl]-5-fluoro-2-methyl-4-pyrimidinyl}hydrazino)-3-oxopropyl]hydroxyformamide (8.15 g, 18.05 mmol, 62.7% yield) as a white solid. LCMS: (M+H)+: 451.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-75a2c1a2509f484d82c06d1e69270597
Source noteuspto-grants-2011_02