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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393451Generated: October 31, 2026

Triethylamine → HCID 86753096, compound

https://huagongshe.com/reaction/2393451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-BenzylpiperazineHCID 75994—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 18975307HCID 18975307—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
ProductHCID 86753096HCID 8675309619%

Reaction Steps

To a suspension of 3-(5-(1,2,4-triazol-4-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl)propionic acid (0.23 g) in dry DMF (3 mL) was added 1-benzylpiperazine (0.1 mL, 0.58 mmol), 1-hydroxybenzotriazole (66 mg, 0.49 mmol), 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (93 mg, 0.49 mmol) and triethylamine (68 μL, 0.4 mmol) and this mixture was stirred at ambient temperature under nitrogen for 24 hours. The solvent was evaporated in vacuo and the residue partitioned between ethyl acetate (25 mL) and water (20 mL). The two phases were separated and the aqueous phase was extracted with ethyl acetate (3×25 mL). The combined organics were dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica eluting with 90:10:1, DCM:MeOH:NH3 to give the title compound (30 mg, 19%) as a colourless solid. mp 185° C. (dec.). 1H NMR (360 MHz, CDCl3 :d4 -MeOH 9:1) δ 2.29-2.34 (2H, m), 2.35-2.42 (2H, m), 2.70 (2H, t, J=7.4Hz), 3.12 (2H, t, J=7.4Hz), 3.36-3.43 (2H, m), 3.48 (2H, s), 3.58-3.64 (2H, m), 7.24-7.35 (5H, m), 7.37 (1H, s), 7.67 (1H, s), 8.60 (1H, s) and 8.93 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807857
Source datasetuspto-grants-1998_09
ORD IDord-091302ab33b849f1be320de000b1f96f
Source noteuspto-grants-1998_09