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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465701Generated: October 30, 2026

2-Fluoro-6-methoxybenzaldehyde → HCID 67517547, compound

https://huagongshe.com/reaction/1465701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-6-methoxybenzaldehydeHCID 2737357—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 67518282HCID 67518282—
SolventMethanolHCID 887—
ProductHCID 67517547HCID 6751754740.3%

Reaction Steps

Added 2-Fluoro-6-methoxy benzaldehyde (69 mg, 0.44 mmol) to a mixture of (R)-5-(5-(piperidin-3-yl)-1H-1,2,4-triazol-3-yl)-3-(pyridin-4-yl)-1H-indazole (96 mg, 0.277 mmol) and sodium triacetoxy borohydride (176 mg, 0.833 mmol) in MeOH (8 ml) at room temperature. After stirred for 30 minutes, the solvent was evaporated. Diluted with EtOAc (150 ml), washed with H2O (50 ml), dried (Na2SO4) and concentrated. Crude product was purified on silica gel eluting with 5% v/v MeOH/CH2Cl2 to yield (R)-5-(5-(1-(2-fluoro-6-methoxybenzyl)piperidin-3-yl)-1H-1,2,4-triazol-3-yl)-3-(pyridin-4-yl)-1H-indazole as a white solid (54 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999966B2
Source datasetuspto-grants-2015_04
ORD IDord-ceef6e827a6840d2981057598614ea1b
Source noteuspto-grants-2015_04