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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105203Generated: November 2, 2026

Methylamine → 6-(N-Methylcarbamoyl)-2-{2-[3-(pyrid-2-yl)isoxazol-5-yl]pyrrolidin-1-yl]-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine

https://huagongshe.com/reaction/2105203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant6-Methoxycarbonyl-2-{2-[3-(pyrid-2-yl)isoxazol-5-yl]pyrrolidin-1-yl}-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidineHCID 11305382—
SolventMethanolHCID 887—
Product6-(N-Methylcarbamoyl)-2-{2-[3-(pyrid-2-yl)isoxazol-5-yl]pyrrolidin-1-yl]-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidineHCID 1139666134%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 6-methoxycarbonyl-2-{2-[3-(pyrid-2-yl)isoxazol-5-yl]pyrrolidin-1-yl}-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine Example 56) (62.5 mg, 0.14 mmol), 2N solution of methylamine in methanol (2.0 ml, 4.00 mmol) and methanol (3.0 ml) was heated at 65° C. for 1 hour under microwave irradiation. The volatiles were removed by evaporation and the residue dissolved in DCM and purified by chromatography on silica gel eluting with DCM/methanol (100:0 increasing in polarity to 90:10). The purified product was triturated with diethylether and the resulting solid collected by filtration to give the title compound (21 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579349B2
Source datasetuspto-grants-2009_08
ORD IDord-cc4e86350d23489e8251af4a53060e6f
Source noteuspto-grants-2009_08