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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255062Generated: October 25, 2026

Dicyclohexylcarbodiimide → Phenyl-phenylamino-acetic acid 1-methyl-azepan-4-yl ester

https://huagongshe.com/reaction/1255062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantalpha-(Phenylamino)benzeneacetic acidHCID 19375—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Methylazepan-4-olHCID 10975509—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl-phenylamino-acetic acid 1-methyl-azepan-4-yl esterHCID 5940125020.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-4e41b03569bf412fa05ed8bb46ee0bc0
Source noteuspto-grants-2013_06