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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77029Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → HCID 59401250, Verbindung

https://huagongshe.com/de/reaction/77029

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Eduktalpha-(Phenylamino)benzeneacetic acidHCID 19375—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1-Methylazepan-4-olHCID 10975509—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59401250HCID 5940125020,3%

Reaktionsschritte

A mixture of 2-phenyl-2-(phenylamino)acetic acid (I1) (175 mg, 0.77 mmol), DCC (192 mg, 0.92 mmol), HOBt (124 mg, 0.92 mmol) and 1-methyl-azepan-4-ol (100 mg, 0.77 mmol) in dry THF (100 mL) is stirred at RT overnight under nitrogen flowstream (UPLC-MS monitoring: complete conversion). The solvent is evaporated and the residue is taken up with aq. HCl and washed with EtOAc. The aqueous phase is basified with NaHCO3 and extracted with DCM (three times). The organic layers are combined, dried over Na2SO4, filtered and evaporated to dryness. The resulting crude is first purified by flash chromatography (DCM to DCM/MeOH=95/5) and then by preparative LC-MS. The purified compound is partitioned between sat. NaHCO3 and DCM, the organic phase is dried over Na2SO4, filtered and evaporated under vacuum to give 53 mg of the title compound as brown oil (20% yield, mixture of diastereoisomers).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835682B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-0605cbee109747b89d917af46f3abb88
Quellennotizuspto-grants-2014_09