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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994157Generated: November 2, 2026

Ethylenediamine → HCID 58674351, compound

https://huagongshe.com/reaction/1994157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantHCID 58674598HCID 58674598—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 58674351HCID 58674351—

Reaction Steps

(E)-N-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(3-(2-cyanopyridin-4-yloxy)phenyl)-2-methylacrylamide (500 mg, 1.09 mmol) and TEA (456 μL, 3.27 mmol) were combined and stirred in ethanol. H2S was bubbled into the solution for 2 min then the reaction mixture was sealed and allowed to stir at rt. Reaction completion was checked by LCMS and TLC. The mixture was diluted with EtOAc and washed with brine. The aqueous phase was extracted with EtOAc, and the organic solutions were combined, dried over Na2SO4, filtered, and concentrated to provide a yellow residue. The residue was redissolved in ethylene diamine (3 mL), heated to 60° C. for 5 min, and then allowed to cool to rt. The mixture was diluted with EtOAc and washed with brine. The aqueous phase was extracted with EtOAc, and the organic solutions were combined, dried over Na2SO4, filtered, and concentrated. Purification by column chromatography (SiO2, 0-10% MeOH with 1% NH4OH in DCM) provided B-12 (415 mg). LCMS, FA: Rt=1.34 min, [MH+ 501.0]. 1H NMR (400 MHz, CD3OD): δ 8.49 (d, 1H), 8.18 (d, 1H), 7.91-7.89 (dd, 1H), 7.57-7.53 (m, 3H), 7.40 (d, 1H), 7.35 (s, 1H), 7.23 (m, 1H), 7.16-7.13 (dd, 1H), 7.09-7.07 (m, 1H), 3.77 (s, 4H), and 2.16 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652041B2
Source datasetuspto-grants-2010_01
ORD IDord-f93415658df142c6a0fdc6f43a7ce5c1
Source noteuspto-grants-2010_01