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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387220Generated: November 1, 2026

Tetrahydrofuran → HCID 21715625, compound

https://huagongshe.com/reaction/1387220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-[(4,6-Dimethoxypyrimidin-2-yl)thio]benzoic acidHCID 2736221—
ReactantHCID 10176119HCID 10176119—
ProductHCID 21715625HCID 21715625—

Reaction Conditions

Temperature45 °C

Reaction Steps

2 g (4,6-dimethoxypyrimidine-2-ylthio)benzoic acid was dissolved in THF, and the solution was added while stirring with 1.22 g N,N′-carbonyldiimidazole at room temperature. The mixture was them stirred for 50 min. at 40-50° C. The solution reacted was fed dropwise while stirring into THF solution of 1.55 g isocyanoethyl acetate at −5° C., immediately after dropping of 2 g DBU at −15° C., and the resulting solution was stirred for two nights at room temperature. After completing the reaction, the solution reacted was poured into ice water, stirred for 30 min. and then extracted with a mixed-solvent consisting of ether and ethyl acetate. The organic layer obtained was washed with water and saturated saline solution in turn and was then dried by using anhydrous magnesium sulfate, and then, the solvent used was removed by distillation under reduced pressure. The residue obtained was purified by using silica gel column chromatography, affording the objective substance in an amount of 1.36 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268310B1
Source datasetuspto-grants-2001_07
ORD IDord-ee7c3ec2c1064acc822ccdcf2eaf5f4a
Source noteuspto-grants-2001_07