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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548525Generated: October 30, 2026

Triethylamine → HCID 178428869, compound

https://huagongshe.com/reaction/548525

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 178481816HCID 178481816—
SolventAcetonitrileHCID 6342—
ProductHCID 178428869HCID 178428869—

Reaction Steps

Under nitrogen, 0.50 g (1.9 mmol) of 3-cyclopropylamino-2-methyl-4-(methylsulfonyl)benzoic acid, 0.24 g (2.4 mmol) of 5-hydroxy-1-methylpyrazole and 0.43 g (2.2 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were dissolved in dry CH3CN. The mixture was stirred at RT for 5 h. 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 1 day. The solvent was removed under reduced pressure, and the residue was taken up in CH2Cl2 and 10% strength H2SO4. The aqueous phase was extracted with CH2Cl2. The organic phases were dried over MgSO4, and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC. This gave 0.19 g of a beige solid of a purity of 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943550B2
Source datasetuspto-grants-2011_05
ORD IDord-062ac8253ba247b99c1a5da4f7fd9318
Source noteuspto-grants-2011_05