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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391634Generated: October 29, 2026

Triethylamine → HCID 178513788, compound

https://huagongshe.com/reaction/391634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantPotassium PermanganateHCID 516875—
ReactantDiaminomaleonitrileHCID 2723951—
ReactantHCID 178511349HCID 178511349—
ReactantHCID 178525780HCID 178525780—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
ProductHCID 178513788HCID 17851378831%

Reaction Steps

1-((Z)-2-Amino-1,2-dicyanovinyl)-3-(trans-4-hydroxycyclohexyl)urea. Trans-4-hydroxycyclohexane carboxylic acid (3.0 g, 20.80 mmol), triethylamine (2.10 g, 20.80 mmol) and diphenylphosphorylazide (5.72 g, 20.80 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 (2.24 g, 21.84 mmol). The solution was heated to 65° C. for 16 h. The resultant heterogeneous mixture was triturated with water. The resultant precipitate was filtered and dried under vacuum to afford the title compound (1.60 g, 31%). MS (ESI) m/z 250.1[M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383634B2
Source datasetuspto-grants-2013_02
ORD IDord-5cf6fa8390ca4ad6be9243863a57f80b
Source noteuspto-grants-2013_02