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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427968Generated: November 2, 2026

Triethylamine → HCID 178513788, compound

https://huagongshe.com/reaction/2427968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantPotassium PermanganateHCID 516875—
ReactantDiaminomaleonitrileHCID 2723951—
ReactantHCID 178511349HCID 178511349—
ReactantHCID 178525779HCID 178525779—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
ProductHCID 178513788HCID 17851378837%

Reaction Steps

1-((Z)-2-Amino-1,2-dicyanovinyl)-3-(trans-4-hydroxycyclohexyl)urea. cis-4-Hydroxycyclohexane carboxylic acid (2.0 g, 13.87 mmol), triethylamine (1.40 g, 13.87 mmol) and diphenylphosphorylazide (3.81 g, 13.87 mmol) were combined in toluene and stirred at room temperature. The reaction was monitored via thin layer chromatography (50% ethyl acetate in hexanes, KMnO4 stain). After 30 min the solution was condensed under reduced pressure and the oil diluted with acetonitrile (30 mL) followed by the addition of diaminomaleonitrile (1.57 g, 14.56 mmol). The solution was heated to 65° C. for 16 h. The solution was condensed under reduced pressure and partitioned between water and ethyl acetate (3×), organics combined, dried over magnesium sulfate, filtered and solvent removed to afford the crude product. The crude oil was purified using Biotage silica gel chromatography (70-100% ethyl acetate in hexanes followed by 10% methanol in ethyl acetate) to afford the title compound (1.90 g, 37%). MS (ESI) m/z 250.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968556B2
Source datasetuspto-grants-2011_06
ORD IDord-db3cccc628cc4ec1989bb1b3f42b1971
Source noteuspto-grants-2011_06