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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044683Generated: October 30, 2026

Water → HCID 178464666, compound

https://huagongshe.com/reaction/1044683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylamineHCID 6341—
ReactantHCID 66933446HCID 66933446—
SolventMethanolHCID 887—
ProductHCID 178464666HCID 17846466633%

Reaction Steps

To a solution of 840 mg 4-amino-N-[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-methylsulfanyl-methylene]-3-fluoro-benzenesulfonamide (crude) in 25 mL MeOH was added 3.43 mL of a 70% aqueous solution of ethylamine. The mixture was stirred for 1 h. at room temperature, water was added, and the mixture was extracted with DCM. The combined organic layers were dried over MgSO4 and evaporated to dryness. The residue was purified by flash chromatography (EA/PA 3:1) to give 260 mg (33% over 2 steps) of 4-amino-N-[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]-3-fluoro-benzenesulfonamide as a brown oil. 1H NMR (400 MHz, CDCl3) δ 1.16 (t, J=7.2 Hz, 3H), 1.57-1.87 (m, 7H), 3.43-3.53 (m, 2H), 3.82 (s, 2H), 4.02-4.07 (m, 2H), 6.77 (t, J=8.4 Hz, 1H), 6.80 (s, 1H), 7.50-7.58 (m, 2H) [NH2 invisible].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563723B2
Source datasetuspto-grants-2013_10
ORD IDord-3518fa5e46074047a6814c135b3f9047
Source noteuspto-grants-2013_10