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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445188Generated: November 2, 2026

Diethylethanolamine → HCID 178510407, compound

https://huagongshe.com/reaction/1445188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylethanolamineHCID 7497—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantEthyl 4-morpholinepropionateHCID 88374—
ReactantPotassium 3-morpholin-4-ylpropanoateHCID 68439679—
Reactant4-Cyano-1h-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid saltHCID 178510383—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178510407HCID 1785104076%

Reaction Steps

To a flask containing 3-morpholin-4-yl-propionic acid potassium salt (94 mg, 0.47 mmol, prepared from 3-morpholin-4-yl-propionic acid ethyl ester exactly as described in Example 7, 4-cyano-1H-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid salt (179 mg, 0.36 mmol, as prepared in Example 14 (b)), EDCI (83 mg, 0.43 mmol), and HOBT (68 mg, 0.5 mmol) was added DMF (4 mL). To the stirred slurry was added DEEA (157 μL, 0.9 mmol) and the reaction was allowed to stir overnight. The reaction was diluted with H2O (10 mL) and extracted with EtOAc (2×25 mL). The combined organic extracts were dried (Na2SO4), concentrated in vacuo and the crude product was purified by silica gel preparative TLC to afford 10.4 mg (6%) of the title compound as a white solid. 1H-NMR (CDCl3; 400 MHz): δ 1.49-1.93 (m, 5H), 2.22-2.31 (m, 3H), 2.52 (br s, 4H), 2.58-2.63 (m, 3H), 2.74-2.76 (m, 4H), 3.10-3.17 (m, 2H), 3.72 (br s, 4H), 3.97-4.02 (m, 2H), 4.76-4.81 (m, 2H), 5.81-5.82 (m, 1H), 6.81-6.82 (m, 1H), 6.99-7.00 (m, 1H), 7.09-7.13 (m, 1H), 7.70 (s, 1H), 8.26 (d, 1H, J=8.2 Hz), 9.51 (s, 1H); Mass spectrum (ESI, m/z): Calcd. for C29H36N6O3, 517.28 M+H), found 517.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662837B2
Source datasetuspto-grants-2010_02
ORD IDord-d65e4a97812d40afbda94c1935f99334
Source noteuspto-grants-2010_02