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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629204Generated: November 1, 2026

Hydrochloric Acid → HCID 57461323, compound

https://huagongshe.com/reaction/1629204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant2-BromoacetamideHCID 69632—
ReactantHCID 67050669HCID 67050669—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventCyclohexaneHCID 8078—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57461323HCID 57461323—

Reaction Steps

Following the procedure for 143, 2-[2-(2,4-difluoro-phenyl)-2H-[1,2,4]triazol-3-yl]-9-piperidin-4-yl-4,5-dihydro-2H-6-oxa-1,2-diaza-benzo[e]azulene hydrochloride was reacted with bromo acetamide. The crude product was subjected flash chromatography (SiO2, gradient 50 to 100% ethyl acetate in cyclohexane). Pure fractions were combined and concentrated diethyl ether. The resultant precipitate in vacuo and the resultant residue dissolved in DCM and treated with 4M HCl in dioxane then was collected by filtration to give 178 as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 9.86 (s, 1 H); 8.48-8.43 (m, 1 H); 8.30 (s, 1 H); 8.05 (s, 1 H); 7.85 (td, J=8.75, 5.93 Hz, 1 H); 7.74-7.63 (m, 2 H); 7.41-7.34 (m, 1 H); 7.22 (d, J=2.30 Hz, 1 H); 7.10 (dd, J=8.45, 2.35 Hz, 1 H); 6.97 (d, J=8.39 Hz, 1 H); 4.22 (t, J=5.00 Hz, 2 H); 3.98 (d, J=4.37 Hz, 2 H); 3.60 (t, J=12.26 Hz, 2 H); 3.24-3.13 (m, 2 H); 3.06 (t, J=4.95 Hz, 2 H); 2.69-2.61 (m, 1 H); 1.87 (s, 4 H). LCMS: RT=7.46 min, M+H+=506

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785626B2
Source datasetuspto-grants-2014_07
ORD IDord-1350d6a2fb364d2c9b5e04675871b677
Source noteuspto-grants-2014_07