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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925612Generated: November 1, 2026

Triethylamine → HCID 178434078, compound

https://huagongshe.com/reaction/1925612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CyanideHCID 9032—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Cyclopropylamino-2-methyl-4-(methylsulfonyl)benzoic acidHCID 57424945—
ReactantHCID 178429390HCID 178429390—
SolventAcetonitrileHCID 6342—
ProductHCID 178434078HCID 178434078—

Reaction Steps

Under nitrogen, 0.50 g (1.9 mmol) of 3-cyclopropylamino-2-methyl-4-(methyl-sulfonyl)benzoic acid, 0.27 g (2.4 mmol) of 1,3-dimethyl-5-hydroxypyrazole and 0.43 g (2.2 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were dissolved in dry acetonitrile. The mixture was stirred at RT for 1 day and allowed to stand for 2 days. 0.52 ml (3.7 mmol) of NEt3, 0.10 ml (0.7 mmol) of Me3SiCN and a spatula tip of KCN were added, and the mixture was stirred at RT for 2 days. The solvent was removed under reduced pressure, and the residue was taken up in CH2Cl2 and 10% strength H2SO4. The organic phase was separated off, the aqueous phase was extracted once with CH2Cl2, the combined organic phases were dried over MgSO4 and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC. This gave 0.16 g of a white-beige amorphous solid in a purity of 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178695B2
Source datasetuspto-grants-2012_05
ORD IDord-b876cf92ba1f469db796a18502f1a3da
Source noteuspto-grants-2012_05