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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189544Generated: November 1, 2026

Sodium Bicarbonate → HCID 86654527, compound

https://huagongshe.com/reaction/1189544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl 2-aminoacetate hydrochlorideHCID 11701227—
Reactant1-(2-Chloropyridin-4-yl)pentane-1,4-dioneHCID 24723724—
SolventDichloromethaneHCID 6344—
ProductHCID 86654527HCID 86654527—

Reaction Conditions

Temperature65 °C

Reaction Steps

A slurry of benzyl 2-aminoacetate hydrochloride (922 mg, 4.57 mmol), 1-(2-chloropyridin-4-yl)pentane-1,4-dione (968 mg, 4.57 mmol), and solid sodium bicarbonate (961 mg, 11.4 mmol) in dichloromethane (15.2 mL) was heated to 45° C. for 14 hours. A significant amount of starting material was observed after 14 hours by LC/MS, so the reaction was heated to 65° C. The reaction was allowed to stir (with occasional monitoring by LCMS) at this temperature for 11 days. The reaction was then allowed to cool down to room temperature and poured onto water and extracted with dichloromethane (3×50 mL), dried (sodium sulfate), filtered, and concentrated to a dark orange residue. Purification was achieved by column chromatography (Luknova 80 g, 20 mL/min) using 5 to 45% ethyl acetate in hexanes over 60 minutes. The product, benzyl 2-(2-(2-chloropyridin-4-yl)-5-methyl-1H-pyrrol-1-yl)acetate was isolated as a light orange oil (890 mg, 2.61 mmol, 57% yield). 1H NMR (400 MHz, CDCl3): δ (ppm) 8.23 (d, 1H), 7.36-7.40 (m, 5H), 7.21 (m, 1H), 7.02 (dd, 1H), 6.37 (d, 1H), 6.07 (d, 1H), 5.25 (s, 2H), 4.64 (s, 2H), 2.22 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674115B2
Source datasetuspto-grants-2014_03
ORD IDord-3c0f9fc41f8949719bddcbb1bd301cee
Source noteuspto-grants-2014_03