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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091322Generated: October 31, 2026

Ammonium Chloride → HCID 66778073, compound

https://huagongshe.com/reaction/2091322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 3-(methylamino)propanoateHCID 541480—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-{[Cyclohexyl(3-methylthieno[3,2-b]pyridin-2-yl)methyl]amino}benzoic acidHCID 66778181—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 66778073HCID 6677807384%

Reaction Steps

To a mixture of 4-{[cyclohexyl(3-methylthieno[3,2-b]pyridin-2-yl)methyl]amino}benzoic acid (300 mg) synthesized in Example A144(5), ethyl 3-(methylamino)propanoate (155 mg), 1-hydroxybenzotriazole monohydrate (181 mg), triethylamine (329 μL) and N,N-dimethylformamide (10 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (226 mg), and the mixture was stirred at room temperature for 1 day. 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 (50-100% ethyl acetate/hexane) to give the title object compound (325 mg, 84%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-a68e2d43737b463a8784a6d684cd9475
Source noteuspto-grants-2013_05