Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243139Generated: October 29, 2026

Tert-butoxycarbonylalanine → [(S)-1-(3-Bromo-2-cyclopropylamino-4-fluorophenylcarbamoyl)ethyl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/243139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Bromo-N2-cyclopropyl-4-fluorobenzene-1,2-diamineHCID 68157591—
SolventDichloromethaneHCID 6344—
Product[(S)-1-(3-Bromo-2-cyclopropylamino-4-fluorophenylcarbamoyl)ethyl]carbamic acid tert-butyl esterHCID 6815839781.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3-bromo-N2-cyclopropyl-4-fluorobenzene-1,2-diamine (759 mg, 3.10 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (644 mg, 3.41 mmol), HOAt (464 mg, 3.41 mmol) and N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (654 mg, 3.41 mmol) in DCM (20 mL) was stirred at 0° C. for 1 h. The reaction mixture was then partitioned between DCM and a saturated solution of NaHCO3. The organic fraction was dried and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-50% EtOAc in cyclohexane) to afford the title compound (1.05 g, 81%) as a pale beige solid. LCMS (Method C): RT 3.66 min [M+H]+ 416.05

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-78ae5010312d45bd813dcf735c14ec4a
Source noteuspto-grants-2014_02