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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178643Generated: October 29, 2026

Trifluoroacetic acid → HCID 178428383, compound

https://huagongshe.com/reaction/2178643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant3-(3H-imidazo[4,5-c]pyridin-2-yl)-5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridineHCID 136193591—
SolventDichloromethaneHCID 6344—
ProductHCID 178428383HCID 17842838343%

Reaction Steps

To a solution of 3-(3H-imidazo[4,5-c]pyridin-2-yl)-5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine (LIX) (0.110 g, 0.26 mmol) in dry DCM (5 mL) was added triethylsilane (0.104 mL, 0.65 mmol) followed by TFA (2.5 mL) and stirred at room temperature for 3 h under nitrogen. The solvent was evaporated under reduced pressure, the residue was taken up water (10 mL), and basified with concentrated NH4OH. The precipitates were filtered, washed by cold water and dried under vacuum at room temperature. The crude product was suspended in DCM (10 mL), sonicated briefly and then heated to boiling for 5 min. The solution was cooled to room temperature and the solids were filtered, washed with DCM and dried under vacuum at room temperature to produce 3-(3H-imidazo[4,5-c]pyridin-2-yl)-5-(4-methylpyridin-3-yl)-1H-pyrazolo[3,4-b]pyridine (29) as a white solid (37 mg, 0.11 mmol, 43% yield). 1H NMR (DMSO-d6) δ ppm 2.33 (s, 3H), 7.45 (d, J=4.78 Hz, 1 H), 7.75 (bd, 1 H), 8.43 (d, J=5.29 Hz, 1 H), 8.54 (bs, 2 H), 8.69-8.82 (m, 3 H), 14.64 (s, 1 H); ESIMS found for C18H13N7 m/z 328.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067939B2
Source datasetuspto-grants-2015_06
ORD IDord-a6454fd5bf49421d938bdcd1a88afd83
Source noteuspto-grants-2015_06