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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854487Generated: October 30, 2026

Ammonium formate → HCID 178419835, compound

https://huagongshe.com/reaction/1854487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 178420309HCID 178420309—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 178419835HCID 17841983584.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

Ammonium formate (0.50 g, 7.9 mmol) and Pearlman's catalyst (0.56 g, 0.79 mmol) were added to a solution of 1-(1-benzylpiperidin-4-yl)-3,6-dihydropyrazolo[4,3-d]pyrrolo[2,3-b]pyridine (0.26 g, 0.791 mmol, Example #24) in MeOH (20 mL). The reaction was heated at about 65° C. for about 1 h then filtered through Celite® and concentrated under reduced pressure. The filtrate was concentrated to afford 1-(piperidin-4-yl)-3,6-dihydropyrazolo[4,3-d]pyrrolo[2,3-b]pyridine (0.161 g, 84%): LC/MS (Table 2, Method a) Rt=1.18 min; MS m/z: 242 (M+H), 240 (M−H)−. The crude product was used directly in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962629B2
Source datasetuspto-grants-2015_02
ORD IDord-5920a60efbe34ae2802f78d22a86035d
Source noteuspto-grants-2015_02