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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250475Generated: October 30, 2026

Triethylamine → HCID 16223018, compound

https://huagongshe.com/reaction/2250475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyrrolidineHCID 31268—
ReactantHCID 16223016HCID 16223016—
SolventDichloromethaneHCID 6344—
ProductHCID 16223018HCID 1622301896%

Reaction Steps

A solution of 3-(3-bromomethyl-4-chloro-phenyl)-5-(3-chlorothiophen-2-yl)-[1,2,4]oxadiazol (0.030 g, 0.077 mmol), pyrrolidine (0.013 mL, 0.16 mmol), Et3N (0.054 mL, 0.39 mmol) and dichloromethane (8.0 mL) was stirred at room temperature for 20 h. The solution was diluted with dichloromethane (30 mL), washed with 10% Na2CO3 (25 mL), dried over Na2SO4, and concentrated. The product was azeotroped with dichloromethane (3×5 mL) and hexanes (2×5 mL) to give 0.028 g (96%) of the title compound as a white solid. 1H NMR (CDCl3): 8.27 (d, 1H, J=1.7 Hz), 7.98 (dd, 1H, J=8.2 and 1.9 Hz), 7.61 (d, 1H, J=5.2 Hz), 7.49 (d, 1H, J=8.5 Hz), 7.13 (d, 1H, J=5.2 Hz), 3.85 (s, 2H), 2.67 (br s, 4H), 1.84 (br s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317029B2
Source datasetuspto-grants-2008_01
ORD IDord-1a7f502a75cd466593e93b1956896e50
Source noteuspto-grants-2008_01