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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783795Generated: October 30, 2026

Triethylamine → HCID 24948592, compound

https://huagongshe.com/reaction/1783795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-AminopyridineHCID 10009—
ReactantHCID 86617456HCID 86617456—
SolventDichloromethaneHCID 6344—
ProductHCID 24948592HCID 2494859232%

Reaction Steps

To a solution of 3-aminopyridine (0.051 g, 0.54 mmol) and triethylamine (0.16 mL, 1.14 mmol) in CH2Cl2 (10 mL) was added 3-(2-morpholin-4-yl-ethyl)-imidazo[1,5-a]pyridine-1-carbonyl chloride hydrochloride (150 mg, 0.45 mmol). The mixture was stirred at ambient temperature for 1 h then washed with sat. aq. NaHCO3 (20 mL). The organic layer was separated and the aqueous layer was extracted with dichloromethane (20 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was chromatographed on silica to yield the title compound (50 mg, 32%). 1H NMR (DMSO-d6) δ 10.05 (1H), 9.05 (1H), 8.45 (1H), 8.28 (2H), 8.15 (1H), 7.35 (1H), 7.20 (1H), 6.94 (1H), 3.58 (4H), 3.26 (2H), 2.80 (2H), 2.45 (4H); m/z (M+H)=352.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501438B2
Source datasetuspto-grants-2009_03
ORD IDord-633e267ffa8f495e9d4e6e640639302f
Source noteuspto-grants-2009_03