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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877287Generated: November 2, 2026

Dimethylacetamide → HCID 59529487, compound

https://huagongshe.com/reaction/1877287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 68513427HCID 68513427—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 59529487HCID 59529487—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution (10 mL) of 4-(cyclohexyl{4-methyl-1-[3-(trifluoromethyl)phenyl]-1H-pyrrol-3-yl}methoxy)benzoic acid (0.43 g) synthesized in Example 300 (1) in dimethylacetamide were added triethylamine (0.14 mL), ethyl 3-aminopropanoate hydrochloride (0.16 g), N-(3-dimethylaminopropyl)-ethylcarbodiimide hydrochloride (0.29 g) and 1-hydroxybenzotriazole monohydrate (0.23 g) at room temperature, and the mixture was stirred at 60° C. for 1 hr. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate and purified by silica gel chromatography (ethyl acetate:hexane=1:1, volume ratio) to give a methyl ester form of the title compound (0.10 g). This was dissolved in ethanol (2 mL), 1N sodium hydroxide (1.5 mL) was added, and the mixture was stirred at room temperature for 1 hr. Ethanol was evaporated under reduced pressure, and 1N hydrochloric acid (1.5 mL) was added to the residue to give the title compound (25.4 mg, 5%) as an amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-e0bc15702da547cabc192a8edf7fd232
Source noteuspto-grants-2012_11