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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581885Generated: November 1, 2026

Sodium Hydroxide → HCID 178476507, compound

https://huagongshe.com/reaction/1581885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant3-[3-(2-Chlorophenylsulfonyloxy)-5-methylphenoxy]propionaldehydeHCID 22722639—
ReactantHCID 178513186HCID 178513186—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178476507HCID 17847650786.9%

Reaction Steps

2-[2-[3-(2-Chlorophenylsulfonyloxy)-5-methylphenoxy]ethyl-1-methylene]hydrazinecarboximidamide hydrochloride: A solution of 289 mg (0.82 mmol) of 3-[3-(2-chlorophenylsulfonyloxy)-5-methylphenoxy]propionaldehyde, as prepared in the preceding step, 223 mg (1.62 mmol) of aminoguanidine nitrate, and 200 μL (0.80 mmol) of 4N HCl/dioxane in 3 mL of ethanol was stirred at ambient temperature overnight. The reaction mixture was treated with 10 mL of water and stirred for 15 min. The reaction mixture was treated with 1.2 mL of 2N sodium hydroxide and then extracted into dichloromethane (3×20 mL). The organic phase was washed with water (3×20 mL), dried (K2CO3), and concentrated to give 321 mg of crude product as a free base. The residue was dissolved in dichloromethane (1 mL), treated with 800 μL (3.2 mmol) of 4N HCl/dioxane solution. The solvent was removed and the product was triturated from a mixture of dichloromethane/ether/hexane to give 190 mg of the title compound as a colorless solid. 1H-NMR (300 MHz, DMSO-d6) δ 11.58 (br s, 1H), 7.95 (dd, 1H, J=7.9, 1.5 Hz), 7.90-7.80 (m, 2H), 7.52-7.61 (m, 6H), 6.77 (s, 1H), 6.49 (s, 1H), 6.46 (br t, 1H, J=2.2 Hz), 4.14 (t, 2H), 2.67 (q, 2H), and 2.21 (s, 3H). Mass spectrum (MALDI-TOF, α-cyano-4-hydroxycinnamic acid matrix) calcd. for C17H19ClN4O4S: 411.1 (M+H). Found: 411.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730783B2
Source datasetuspto-grants-2004_05
ORD IDord-a760793a0c6b4959af4c0bee938df71f
Source noteuspto-grants-2004_05