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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515816Generated: October 31, 2026

Ethyl orthoformate → HCID 86683477, compound

https://huagongshe.com/reaction/515816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 86683478HCID 86683478—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86683477HCID 8668347737.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-(5-(4-amino-3-hydroxyphenyl)-8-oxo-6-thioxo-5,7-diazaspiro[3.4]octan-7-yl)-3-(trifluoromethyl)picolinonitrile (60 mg, 0.14 mmol) and triethylorthoformate (0.050 mL, 0.28 mmol) in anhydrous DMF (1 mL) was heated at 100° C., 1 h. The mixture was diluted with water, extracted with EtOAc (3×), the organics combined and washed with water (2×), brine, dried (MgSO4) and concentrated. Purification by column chromatography, eluting with 30% EtOAc/hexanes provided 23 mg of 5-(5-(benzo[d]oxazol-6-yl)-8-oxo-6-thioxo-5,7-diazaspiro[3.4]octan-7-yl)-3-(trifluoromethyl)picolinonitrile as a pale yellow solid. 1H NMR (300 MHz, DMSO-d6) δ 9.24 (d, 1H), 8.95 (s, 1H), 8.78 (d, 1H), 8.05 (d, 1H), 7.94 (d, 1H), 7.45 (dd, 1H), 2.74-2.61 (m, 2H), 2.59-2.47 (m, 2H), 2.03-1.90 (m, 1H), 1.61-1.48 (m, 1H). LCMS [M+1]+ 444.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108944B2
Source datasetuspto-grants-2015_08
ORD IDord-0a11d3819bee44b6934f3b924b3dc399
Source noteuspto-grants-2015_08