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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091278Generated: November 2, 2026

Dimethylformamide → HCID 66777637, compound

https://huagongshe.com/reaction/2091278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 3-(methylamino)propanoateHCID 541480—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 66777853HCID 66777853—
SolventTriethylamineHCID 8471—
ProductHCID 66777637HCID 6677763770%

Reaction Steps

To a mixture of 4-[(cyclohexyl{5-fluoro-3-[(2-methoxyethoxy)methyl]-1-benzofuran-2-yl}methyl)amino]benzoic acid (200 mg) synthesized in Example A132(6), ethyl 3-(methylamino)propanoate (86.4 mg), 1-hydroxybenzotriazole monohydrate (101 mg), triethylamine (184 μL) and N,N-dimethylformamide (10 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (126 mg), and the mixture was stirred overnight at room temperature. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30-70% ethyl acetate/hexane) to give the title object compound (175 mg, 70%) as a pale-brown oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-9b70a0cc01804dcdb5f862893cc149a1
Source noteuspto-grants-2013_05