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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420512Generated: October 30, 2026

Hydrochloric Acid → HCID 57906509, compound

https://huagongshe.com/reaction/420512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 66659119HCID 66659119—
Catalyst1,4-DioxaneHCID 31275—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57906509HCID 5790650924.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

In a sealed flask, a solution of 6-(2,4-dichloro-phenyl)-8-isobutylamino-imidazo[1,2-a]pyridine-7-carbonitrile (19.1 mg, 0.053 mmol) in THF (0.5 mL) was cooled to 0° C. (ice bath), treated with BH3.THF complex (1.0 M solution in THF, 0.48 mL, 0.48 mmol) and heated at 40° C. After 1 h, the reaction was not complete according to HPLC. 4.0 M HCl in dioxane (2 drops) and additional BH3.THF complex (1.0 M solution in THF, 0.16 mL, 0.16 mmol) were added, then the reaction mixture was heated at 40° C. for 14 h, cooled to 0° C., and diluted in MeOH (large excess). The resulting mixture was concentrated under vacuum, and the remaining residue was dissolved in TFA. After evaporation to dryness, the remaining residue was purified by reverse phase prep-HPLC (Waters system) to give the title compound (2TFA salt, 7.6 mg, 0.013 mmol, 24%). MS: 363 [M+1]+; HPLC: AtRet=1.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097617B2
Source datasetuspto-grants-2012_01
ORD IDord-b093f44e4e7741d39044f0ebf871fbac
Source noteuspto-grants-2012_01