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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484465Generated: October 25, 2026

1H-Indole-5-sulfonamide → HCID 178464642, compound

https://huagongshe.com/reaction/1484465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-5-sulfonamideHCID 21683100—
ReactantN-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl esterHCID 53354231—
SolventAcetonitrileHCID 6342—
ProductHCID 178464642HCID 17846464287%

Reaction Steps

100 mg (1 mol equiv.) N-Ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester and 92.5 mg (1.05 mol equiv.) 1H-indole-5-sulfonic acid amide were added to 3 mL acetonitrile. The reaction mixture was refluxed overnight and volatiles were removed under reduced pressure. The residue was taken up in ethyl acetate and extracted with 2N NaOH. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. Purification by flash chromatography on silica gel (Et2O:EtOAc=1:1) afforded 152 mg (87%) 1H-indole-5-sulfonic acid (2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methyleneamide. 1H NMR (400 MHz, CDCl3) δ 1.14 (t, J=7.2 Hz, 3H), 1.59-1.79 (m, 8H), 3.43-3.51 (m, 2H), 3.79 (br.s., 2H), 6.63-6.65 (m, 1H), 6.76 (s, 1H), 6.99 (br.s., 1H), 7.30 (t, J=2.8 Hz, 1H), 7.43 (d, J=8.6 Hz, 1H), 7.76 (dd, J=8.6, 1.8 Hz, 1H), 8.27 (br.s., 1H), 8.54 (br.s., 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422244B2
Source datasetuspto-grants-2016_08
ORD IDord-8a2f8b2419a246669fe99ede3e634c33
Source noteuspto-grants-2016_08