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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242770Erstellt: 26. Oktober 2026

4-Methylmorpholine → HCID 68157517, Verbindung

https://huagongshe.com/reaction/242770

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktN-carbobenzyloxyalanineHCID 736104—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt3-Methyl-N2-phenyl-1,2-benzenediamineHCID 68157147—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 68157517HCID 6815751790,5%

Reaktionsschritte

To a solution of 3-methyl-N2-phenyl-benzene-1,2-diamine (852 mg, 4.3 mmol) in anhydrous DCM (20 mL) were added (S)-2-benzyloxycarbonylaminopropionic acid (1.44 g, 6.45 mmol), HOBt (639 mg, 4.73 mmol), 4-methylmorpholine (1.04 mL, 9.46 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.24 g, 6.45 mmol). The mixture was stirred at RT for 6.5 h and then partitioned between DCM (100 mL) and water. The organic layer was then washed with brine, dried (Na2SO4) and concentrated in vacuo. The resulting residue was dissolved in AcOH (10 mL) and heated to 65° C. for 18 h. After cooling to RT, volatiles were removed under reduced pressure and the residue diluted with EtOAc (100 mL). The organic layer was washed with a saturated solution of NaHCO3, followed by brine, then dried (Na2SO4) and concentrated in vacuo affording [(S)-1-(7-Methyl-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid benzyl ester as brown foam (1.5 g, 90%). LCMS: RT 3.07 min [M+H]+ 386.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653089B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-5d92de7fe1a84244b88539d299b4d77a
Quellennotizuspto-grants-2014_02