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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808849Generated: October 30, 2026

4-Cyanobenzoic acid → HCID 57345433, compound

https://huagongshe.com/reaction/1808849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzoic acidHCID 12087—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 67773410HCID 67773410—
SolventDichloromethaneHCID 6344—
ProductHCID 57345433HCID 5734543349%

Reaction Steps

4-cyanobenzoic acid (65.0 mg, 0.44 mmol) in DCM (2 mL) was treated with DIPEA (0.231 mL, 1.32 mmol) and TBTU (142 mg, 0.44 mmol) and the suspension was stirred for 10 min. A 125 mg/mL solution of (S)-1-(2-cyclohexyl-2-(methylamino)ethyl)azetidin-3-ol (Compound G2.3) (125 mg, 0.44 mmol) in DCM (1 mL) was added and the reaction was stirred at ambient temperature overnight. The reaction was washed with 8% aq. sol. of NaHCO3 and concentrated. The residue was dissolved in DMSO (0.4 mL) and filtered through a syringe filter. The residue was purified by HPLC to give the title compound (73.6 mg, 49%). Mixture of rotamers. 1H NMR (600 MHz, DMSO-d6) δ 0.53-0.70, 0.89-1.81, 2.43-2.59, 2.64-2.78, 3.03, 3.28-3.31, 3.43-3.54, 4.11-4.30, 5.23, 5.26, 7.48, 7.61, 7.87-7.94. HRMS (M+H)+: calculated 342.2181. found 342.2193

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361998B2
Source datasetuspto-grants-2013_01
ORD IDord-20e6240c5bd34d8b9af0b1b047d6edae
Source noteuspto-grants-2013_01