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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091298Generated: November 1, 2026

Ammonium Chloride → HCID 66777167, compound

https://huagongshe.com/reaction/2091298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 86761829HCID 86761829—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 66777167HCID 6677716780.5%

Reaction Steps

To a mixture of 4-{[cyclohexyl(3-methylthieno[3,2-c]pyridin-2-yl)methyl]amino}benzoic acid (211 mg) synthesized above, β-alanine ethyl ester hydrochloride (128 mg), 1-hydroxybenzotriazole monohydrate (128 mg), triethylamine (233 μL) and N,N-dimethylformamide (10 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (160 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 aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (60-100% ethyl acetate/hexane) to give the title object compound (214 mg, 80%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-09ed6bd3b79b4f8c95461071059c748e
Source noteuspto-grants-2013_05