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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783798Generated: October 25, 2026

1,2-Dichloroethane → HCID 24948783, compound

https://huagongshe.com/reaction/1783798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantMemantine HydrochlorideHCID 181458—
Reactant3-Butyl-imidazo[1,5-a]pyridine-1-carboxylic acidHCID 24948397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 24948783HCID 2494878316%

Reaction Steps

To a solution of 3-butyl-imidazo[1,5-a]pyridine-1-carboxylic acid (200 mg, 0.73 mmol) in DMF (5 mL) was added EDC (182 mg, 0.95 mmol), HOBt, (129 mg, 0.95 mmol) and iPr2EtN (0.22 mL, 1.31 mmol). The mixture was allowed to stir for 10 min. and 3,5-dimethyl-1-aminoadamantane hydrochloride (187 mg, 0.88 mmol) was added. The mixture was stirred for 15 h then diluted with ethyl acetate (30 mL) and washed with water (50 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was chromatographed on silica to yield the title compound (50 mg, 16%). 1H NMR (DMSO-d6) δ 8.32 (1H), 8.00 (1H), 7.05 (1H), 6.95 (1H), 6.81 (1H), 3.55 (4H), 3.15 (2H), 2.73 (2H), 2.45 (4H), 2.11 (1H), 1.90 (2H), 1.73 (4H), 1.30 (4H), 1.75 (2H), 0.85 (6H); m/z (M+H)=437.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501438B2
Source datasetuspto-grants-2009_03
ORD IDord-8a887097a529414d9485b425ba8bbeba
Source noteuspto-grants-2009_03