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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365729Generated: October 30, 2026

Ethanol sodium ethoxide → HCID 58962289, compound

https://huagongshe.com/reaction/1365729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol sodium ethoxideHCID 23706232—
ReactantHCID 58962311HCID 58962311—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58962289HCID 5896228986.2%

Reaction Steps

To a stirred suspension of ethyl 3′-(methylsulfonyloxy)-4′-oxo-6′,7′-dihydro-4′H-spiro[cyclopentane-1,9′-pyrimido[2,1-c][1,4]oxazine]-2′-carboxylate (0.6861 g, 1.84 mmol) in THF (50 mL) was added 1M EtONa/EtOH (10 mL). After 1 h, the resulting yellow solution was concentrated, acidified with 1 M aq. HCl (20 mL), extracted with CH2Cl2 (3×35 mL). The combined organic layers dried (Na2SO4), filtered and concentrated to give the title compound as a brown solid (0.4668 g, 86%). 1H NMR (500 MHz, CDCl3) δ: 10.49 (1H, s), 4.44 (2H, q, J=7.0 Hz), 4.03-3.97 (4H, m), 2.28-2.22 (2H, m), 2.06-2.01 (2H, m), 1.93-1.81 (4H, m), 1.42 (3H, t, J=7.0 Hz). HRMS (M+H) calcd for C14H19N2O5: 295.1294; found: 295.1293.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893055B2
Source datasetuspto-grants-2011_02
ORD IDord-ccc50472be7a4f4fa2b990230068c13f
Source noteuspto-grants-2011_02