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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828549Generated: October 30, 2026

Trichloroacetyl isocyanate → HCID 86588152, compound

https://huagongshe.com/reaction/1828549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl isocyanateHCID 76400—
ReactantSodium FormateHCID 2723810—
ReactantChloroform methanolHCID 21584188—
ReactantHCID 86588150HCID 86588150—
SolventEthyl AcetateHCID 8857—
ProductHCID 86588152HCID 86588152137.6%

Reaction Steps

The tert-butyl (E)-3-{7-fluoro-2-(3-hydroxypiperidino)-8-[2-(4-isopropyl-1,3-thiazol-2-yl)ethyl]-4-oxo-4H-pyrido[1,2-a]pyrimidin-3-yl}-2-propenoate (48.0 mg, 0.0885 mmol) obtained in Example 156, (M) was dissolved in ethyl acetate (3 ml), added with trichloroacetyl isocyanate (0.052 ml, 0.442 mmol) and stirred at room temperature for 1 hour. The reaction mixture was added with methanol:chloroform (1:10, 10 ml) and concentrated, and the resulting residue was dissolved in a mixed solvent of methanol (3 ml) and distilled water (1 ml), added with sodium formate (12.0 mg, 0.177 mmol) and stirred overnight at room temperature. The solution was further added with sodium formate (12.0 mg, 0.177 mmol), stirred for 5 hours and then concentrated, and the resulting residue was purified by preparative TLC (chloroform:methanol=100:5) to obtain the title compound (71.3 mg, quantitative) as lyophilized product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056917B2
Source datasetuspto-grants-2006_06
ORD IDord-ffc65b0a625941d1bd4abac445eeb248
Source noteuspto-grants-2006_06