Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366486Generated: October 29, 2026

[(2R)-2-(cyclopentylmethyl)-3-(2-{5-fluoro-6-[(4S)-4-hydroxy-3,3-dimethyl-1-pyrrolidinyl]-2-methyl-4-pyrimidinyl}hydrazino)-3-oxopropyl][(phenylmethyl)oxy]formamide → HCID 58000678, compound

https://huagongshe.com/reaction/1366486

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(2R)-2-(cyclopentylmethyl)-3-(2-{5-fluoro-6-[(4S)-4-hydroxy-3,3-dimethyl-1-pyrrolidinyl]-2-methyl-4-pyrimidinyl}hydrazino)-3-oxopropyl][(phenylmethyl)oxy]formamideHCID 86636958—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 58000678HCID 5800067890%

Reaction Steps

To a solution of [(2R)-2-(cyclopentylmethyl)-3-(2-{5-fluoro-6-[(4S)-4-hydroxy-3,3-dimethyl-1-pyrrolidinyl]-2-methyl-4-pyrimidinyl}hydrazino)-3-oxopropyl][(phenylmethyl)oxy]formamide (0.1606 g, 0.296 mmol) in MeOH (5 mL) was added 10% Pd/C (50% water, 48 mg). The mixture was hydrogenated under balloon pressure for 1 h, and was then filtered. The solution was concentrated in vacuo and the residue was crystallized from EtOAc-hexanes to afford [(2R)-2-(cyclopentylmethyl)-3-(2-{5-fluoro-6-[(4S)-4-hydroxy-3,3-dimethyl-1-pyrrolidinyl]-2-methyl-4-pyrimidinyl}hydrazino)-3-oxopropyl]hydroxyformamide (0.1205 g, 90% yield) as a light pink solid. LCMS: (M+H)+: 453.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-89632ec67b254d7088f9f435a452bae3
Source noteuspto-grants-2011_02