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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714835Generated: October 30, 2026

Water → HCID 117840290, compound

https://huagongshe.com/reaction/714835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantHCID 117840151HCID 117840151—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117840290HCID 11784029075.1%

Reaction Steps

To a solution of (3S)-1-(2-((1-(1-amino-2-methylpropan-2-yl)-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)-3-cyclopropyl-2-oxopyrrolidine-3-carbonitrile dihydrochloride (100 mg) obtained in Example 115 in tetrahydrofuran (5 mL) were added successively dropwise triethylamine (0.15 mL) and methoxyacetyl chloride (26 mg) at 0° C. under nitrogen atmosphere, and the mixture was stirred at room temperature for 5 hr. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol). To a solution of the residue (89 mg) in ethanol (5.0 mL) was added 1 M hydrochloric acid (0.20 mL), and the mixture was stirred at room temperature for 5 min. The solvent was evaporated under reduced pressure, and the residue was recrystallized (diisopropyl ether/ethyl acetate) to give the title compound (81 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187453B2
Source datasetuspto-grants-2015_11
ORD IDord-7b444c3c906e4ed2af493da41a531700
Source noteuspto-grants-2015_11