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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044352Generated: October 30, 2026

Hydrochloric Acid → HCID 58204645, compound

https://huagongshe.com/reaction/2044352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58204289HCID 58204289—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 58204645HCID 58204645—

Reaction Steps

A solution of 2-[2-(2,2,2-trifluoro-ethyl)-2H-[1,2,4]triazol-3-yl]-4,5-dihydro-6-oxa-1,10b-diaza-benzo[e]azulene-9-carbaldehyde (175 mg, 0.48 mmol) and piperazine ethanol in DCE (15 mL) was treated with sodium triacetoxyborohydride (153 mg, 0.72 mmol) and catalytic acetic acid and then stirred at RT for 72 h. The resultant mixture was diluted with DCM and washed with saturated aqueous sodium hydrogen carbonate then dried (Na2SO4), filtered and concentrated in vacuo to give a colourless gum which was subjected to flash chromatography (SiO2, gradient 0-10% MeOH in DCM). The appropriate fractions were combined, concentrated in vacuo and the resultant residue dissolved in diethyl ether and treated with 1M HCl in diethyl ether (2 mL, 2 mmol). The resultant precipitate was filtered off, washed with ether and dried in vacuo to give 128 as a white solid. 1H NMR (DMSO-d6 plus deuterated TFA, 400 MHz): δ 8.22 (s, 1H); 8.16-8.12 (m, 1H); 7.66-7.60 (m, 1H); 7.39 (d, J=8.3 Hz, 1H); 7.02 (s, 1H); 5.75 (q, J=8.7 Hz, 2H); 4.57 (t, J=5.9 Hz, 2H); 4.52 (s, 2H); 3.76 (t, J=5.0 Hz, 2H); 3.61 (br s, 8H); 3.32 (s, 2H); 3.24 (t, J=5.9 Hz, 2H). 1 Exchangeable not observed. LCMS: RT=6.56 min, M+H+=478

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586574B2
Source datasetuspto-grants-2013_11
ORD IDord-8c3931e8215f40b4bb708dd3e698726b
Source noteuspto-grants-2013_11