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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889634Generated: October 31, 2026

Water → HCID 66616612, compound

https://huagongshe.com/reaction/1889634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-FluorobenzylamineHCID 67326—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 66616568HCID 66616568—
SolventEthyl AcetateHCID 8857—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
ProductHCID 66616612HCID 66616612105.1%

Reaction Steps

To a solution of 4′-fluoro-5-(methoxycarbonyl)biphenyl-3-carboxylic acid (400 mg, 1.459 mmol) in DMF/CH2Cl2 at rt was added EDCI.HCl (363 mg, 1.896 mmol) followed by HOBt.H2O (197 mg, 1.459 mmol). After one minute, (4-fluorophenyl)methanamine (183 mg, 1.459 mmol) was added to the mixture and the reaction mixture was stirred at rt for 4 h. To the reaction mixture were added EtOAc and aq. NaHCO3. The EtOAc layer was separated, washed with water, dried over MgSO4 and concentrated in vacuo to obtain a crude product as a light yellow solid (585 mg, >100% yield), MS: M+H=382.21. The crude product was used directly in the next step without further purification. 1H NMR (CDCl3): δ 8.39 (s, 1H), 8.32 (s, 1H), 7.58˜7.02 (m, 9H), 4.63 (d, J=6.0 Hz, 2H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-467034407867456dbe04df494c32b000
Source noteuspto-grants-2013_08