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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640390Generated: November 2, 2026

Hydrochloric Acid → HCID 178428871, compound

https://huagongshe.com/reaction/1640390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantPotassium CyanideHCID 9032—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 66738910HCID 66738910—
ReactantHCID 178481816HCID 178481816—
CatalystAcetone CyanohydrinHCID 6406—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 178428871HCID 178428871—

Reaction Steps

90 mg (0.91 mmol) of 5-hydroxy-1-methylpyrazole and a spatula tip of 4-(dimethylamino)pyridine were added to 230 mg (0.83 mmol) of 2-methyl-3-methylsulfinyl-4-methylsulfonylbenzoic acid in 20 ml of CH2Cl2. 191 mg (0.99 mmol) of 1-(3′-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were added, and the mixture was stirred at RT for 90 min. 3 ml of 1M HCl were then added, and the organic phase was freed from the solvent. 168 mg (1.66 mmol) of triethylamine, 10 drops of acetone cyanohydrin and a spatula tip of potassium cyanide were added to the residue in 15 ml of acetonitrile. The reaction mixture was stirred at RT for 16 h and then freed from the solvent. 15 ml of CH2Cl2 were added to the residue, and 2 ml of 1M HCl were then added. After phase separation, the organic phase was freed from the solvent. The residue was stirred with 25 ml of a mixture of aqueous saturated sodium bicarbonate solution and diethyl ether at RT for 10 min. The phases were separated, and the aqueous phase was acidified with dilute HCl and then extracted three times with CH2Cl2. The combined organic phases were freed from the solvent. This gave 171 mg of clean product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114816B2
Source datasetuspto-grants-2012_02
ORD IDord-cdaf1d0a1fd448439dc3b5469f278c45
Source noteuspto-grants-2012_02