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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497468Generated: November 2, 2026

Triethylamine → HCID 69747523, compound

https://huagongshe.com/reaction/497468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(3-Isocyanatophenyl)ethan-1-oneHCID 312718—
ReactantHCID 69750542HCID 69750542—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69747523HCID 6974752338.3%

Reaction Steps

In a dry flask (3R,4S)-3-amino-4-[(S)-3-(4-fluoro-benzyl)-piperidine-1-carbonyl]-piperidine-1-carboxylic acid t-butyl ester (77 mg, 0.18 mmol) was dissolved in tetrahydrofuran (2.5 mL) and triethylamine (20 μL, 0.143 mmol) and 3-acetylphenylisocyanate (50 μL, 0.36 mmol) were added. The reaction mixture was stirred for 16 hours. The reaction mixture was concentrated in vacuo and purified by preparative reverse-phase HPLC (10-90% acetonitrile in water with 0.05% trifluoroacetic acid) to give a white amorphous solid (40 mg, 38%). 1H NMR (300 MHz, CDCl3), δ: 7.98 (d, J=8, 1H), 7.83 (m, 2H), 7.74 (m, 1H), 7.65 (m, 2H), 7.56 (m, 1H), 7.46 (m, 1H), 7.01 (m, 2H), 6.87 (m, 1H), 3.09 (m, 1H), 2.51-2.77 (m, 7H), 2.42 (m, 1H), 1.23-1.78 (m, 1H), 1.42 (s, 9H). HRMS (ESI), C32H42FN4O5 m+/z: calc.=581.3139, found=581.3142.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949546B2
Source datasetuspto-grants-2005_09
ORD IDord-2c0a97fec5b444319634d55cf418ab9a
Source noteuspto-grants-2005_09