Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594936Generated: October 31, 2026

o-Fluorobenzaldehyde → HCID 86689211, compound

https://huagongshe.com/reaction/594936

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSodiumHCID 5360545—
ReactantHCID 86689212HCID 86689212—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 86689211HCID 86689211—

Reaction Steps

In a flask, dichloromethane (0.295 mL) and acetic acid (2 drops) was added to N-(piperidin-3-yl)-3-(pyridin-4-yl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxamide trifluoroacetate salt (0.021 g, 0.05 mmol) and 2-fluorobenzaldehyde (0.0124 g, 0.1 mmol). The reaction was sonicated for 1 hr. Sodium triacetoxyborohydride (0.050 g, 0.25 mmol) was added in one portion. The reaction was stirred for an additional 16 hours. Saturated sodium bicarbarbonate (1 mL) was added. The reaction was stirred for an additional 5 minutes and was extracted with dichloromethane (3×1 mL). The extracts were combined, dried with anhydrous sodium sulfate, filtered, and concentrated in vacuo. The resulting crude product was purified by prep LC/MS. LC-MS: 435.68 [M+H]. LC/MS RT=1.82 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242981B2
Source datasetuspto-grants-2016_01
ORD IDord-0b233736ecec4724b6d0450a838e663f
Source noteuspto-grants-2016_01