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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510375Generated: October 30, 2026

Ethyl 3-(oxan-4-yl)-3-oxopropanoate → HCID 178515695, compound

https://huagongshe.com/reaction/510375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(oxan-4-yl)-3-oxopropanoateHCID 23144053—
ReactantHCID 86724870HCID 86724870—
SolventAcetic AcidHCID 176—
ProductHCID 178515695HCID 178515695—

Reaction Steps

To a suspension of 4-[(2,3-dichlorophenyl)methyl]-5-(trifluoromethyl)-1H-pyrazol-3-amine TFA salt (201 mg, 0.48 mmol) in acetic acid (2 mL) was added ethyl 3-oxo-3-(tetrahydro-2H-pyran-4-yl)propanoate (100 mg, 0.50 mmol). The reaction vessel was sealed, stirred and irradiated (microwave) at 140° C. for 40 minutes. The reaction mixture was cooled and diluted with acetic acid (5 mL). It was stood still overnight. The precipitate was collected, washed with acetic acid (2 mL), then with cooled methanol (2 mL) and dried to give crude product. The crude material was purified by reverse-phase HPLC to provide titled compound. (16 mg, 7.5%); LC/MS: MS (ES+) m/e 446 (MH+); 1H NMR (400 MHz, DMSO-d6) δ ppm 1.75-1.77 (m, 4H) 2.82 (s, 1H) 3.38-3.41 (m, 2H) 3.96 (dd, J=10.99, 2.91 Hz, 2H) 4.21 (s, 2H) 5.84 (s, 1H) 6.77-6.83 (m, 1H) 7.25 (t, J=7.96 Hz, 1H) 7.54 (dd, J=7.96, 1.39 Hz, 1H) 12.22 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096605B2
Source datasetuspto-grants-2015_08
ORD IDord-af7e6ec1fc234a9aa47a3ef3c9056657
Source noteuspto-grants-2015_08