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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362356Generated: October 30, 2026

Sodium Carbonate → (3-Cyanopyridin-2-ylamino)-acetic acid ethyl ester

https://huagongshe.com/reaction/1362356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-ChloronicotinonitrileHCID 81079—
ReactantPotassium FluorideHCID 522689—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(3-Cyanopyridin-2-ylamino)-acetic acid ethyl esterHCID 1445621851%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-Chloro-3-cyanopyridine (10.0 g, 72 mmol) was dissolved into anhydrous DMSO (200 ml). Glycine ethyl ester hydrochloride (11 g, 79 mmol) and sodium carbonate (4.5 g, 42 mmol) were added and the mixture was stirred for 10 min under argon. Potassium fluoride (4.2 g, 72 mmol) was added and the mixture was heated to 120° C. for 48 h. The mixture was cooled to room temperature and added to water (400 mL). The crude product was extracted with CH2Cl2 (4×100 mL), dried over MgSO4 and concentrated to an orange solid which was purified by silica gel (CH2Cl2) to give an orange solid (7.5 g, 51%). 1H NMR (300 MHz, CDCl3) δ 8.27 (dd, J=5.0, 2.0 Hz, 1H), 7.69 (dd, J=7.6, 2.0 Hz, 1H), 6.66 (dd, J=7.6, 5.0 Hz, 1H), 5.70 (bs, 1H), 4.21-4.28 (m, 4H), 1.29 (t, J=7.2 Hz, 3H); ESI MS m/z 206 [C10H11N3O2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-1c6d40420ac64d4cbc57ba179d99d3f9
Source noteuspto-grants-2011_02