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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783800Generated: October 26, 2026

1,2-Dichloroethane → HCID 24948785, compound

https://huagongshe.com/reaction/1783800

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzylamineHCID 7504—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Butyl-imidazo[1,5-a]pyridine-1-carboxylic acidHCID 24948397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 24948785HCID 2494878517%

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 benzylamine (0.096 mL, 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 (45 mg, 17%). 1H NMR (DMSO-d6) δ 8.43 (1H), 8.28 (1H), 8.07 (1H), 7.26 (4H), 7.20 (1H), 7.05 (1H), 6.85 (1H), 4.44 (2H), 3.48 (4H), 3.20 (2H), 2.80 (2H), 2.45 (4H); m/z (M+H)=365.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501438B2
Source datasetuspto-grants-2009_03
ORD IDord-2b302df757bf4a429cfee724706eadec
Source noteuspto-grants-2009_03