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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838873Generated: October 31, 2026

2-Propanamine, 1-methoxy-, (2S)- → 4-{4-(4-fluorophenyl)-2-methyl-3-oxo-5-[2-(2-methoxy-1-(S)-methyl-ethylamino)-pyrimidin-4-yl]-2,3-dihydro-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1838873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propanamine, 1-methoxy-, (2S)-HCID 7021536—
Reactant4-[4-(4-Fluorophenyl)-2-methyl-5-(2-methanesulfonyl-pyrimidin-4-yl)-3-oxo-2,3-dihydro-pyrazol-1-yl]-piperidine-1 carboxylic acid tert-butyl esterHCID 60061131—
SolventTolueneHCID 1140—
Product4-{4-(4-fluorophenyl)-2-methyl-3-oxo-5-[2-(2-methoxy-1-(S)-methyl-ethylamino)-pyrimidin-4-yl]-2,3-dihydro-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl esterHCID 60061142—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-[4-(4-fluorophenyl)-2-methyl-5-(2-methanesulfonyl-pyrimidin-4-yl)-3-oxo-2,3-dihydro-pyrazol-1-yl]-piperidine-1 carboxylic acid tert-butyl ester, 12, (6 g, 12 mmol) in toluene (30 mL) is added (S)-2-amino-3-methoxypropane (2.14 g, 24 mmol). After stirring at 90° C. for 2 hours, the reaction mixture is cooled to room temperature and then concentrated in vacuo. Purification over silica (50% EtOAc/hexane) affords the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677337B2
Source datasetuspto-grants-2004_01
ORD IDord-cea8d7af68f44d30855fdb8c67e28fba
Source noteuspto-grants-2004_01