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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242972Generated: October 26, 2026

Triethylamine → [(S)-1-(3-Phenylaminopyridin-2-ylcarbamoyl)ethyl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/242972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN3-Phenylpyridine-2,3-diamineHCID 68018423—
SolventDichloromethaneHCID 6344—
Product[(S)-1-(3-Phenylaminopyridin-2-ylcarbamoyl)ethyl]carbamic acid tert-butyl esterHCID 68156995119.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (1.5 mL, 11.0 mmol) was added to a mixture of N3-phenylpyridine-2,3-diamine (510 mg, 2.75 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (0.94 g, 4.96 mmol), HOAt (670 mg, 4.96 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.95 g, 4.96 mmol) in anhydrous DCM (30 mL) at 0° C. under a nitrogen atmosphere. The reaction mixture was stirred at 0° C. for 10 min then slowly warmed to RT. Stirring at RT was continued for 18 h. The reaction mixture was partitioned between DCM and a saturated aqueous solution of NaHCO3. The aqueous phase was further extracted with DCM (×3) and the combined organic fractions washed with water, dried (Na2SO4) and concentrated in vacuo to afford the title compound as a light brown foam (1.17 g, quantitative). LCMS (Method C): RT 3.04 min [M+H]+ 357.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-6dcae8cfbd1d486e830b3fd87d3e6bd1
Source noteuspto-grants-2014_02