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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192956Generated: November 1, 2026

Dimethylamine, hydrochloride → HCID 131730107, compound

https://huagongshe.com/reaction/2192956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-({(2r)-2-[3-Cyclopropyl-4-(cyclopropylsulfonyl)phenyl]-3-[(1r)-3-oxocyclopentyl]propanoyl}amino)pyrazine-2-carboxylic acidHCID 59570880—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 131730107HCID 13173010758%

Reaction Steps

To a solution of 5-({(2R)-2-[3-cyclopropyl-4-(cyclopropylsulfonyl)phenyl]-3-[(1R)-3-oxocyclopentyl]propanoyl}amino)pyrazine-2-carboxylic acid (102 mg), 1-hydroxybenzotriazole (44 mg), and N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide monohydrochloride (59 mg) in DMF (5 mL) were added dimethylamine monohydrochloride (22 mg) and triethylamine (0.09 mL) at room temperature. The reaction mixture was stirred at room temperature overnight, and water was then added thereto for liquid separation. The organic layer was sequentially washed with 1 M hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated brine, and dried over anhydrous magnesium sulfate. The crude product obtained by concentration was purified by silica gel column chromatography (wetting with hexane:ethyl acetate=1:1, chloroform:methanol=1:0-10:1) to obtain 5-({(2R)-2-[3-cyclopropyl-4-(cyclopropylsulfonyl)phenyl]-3-[(1R)-3-oxocyclopentyl]propanoyl}amino)-N,N-dimethylpyrazine-2-carboxyamide (64 mg) as a pale yellow amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329707B2
Source datasetuspto-grants-2012_12
ORD IDord-e51a0a18ece3420490d32531f60e49e8
Source noteuspto-grants-2012_12