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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19934Generated: October 28, 2026

HCID 21976895, compound → 4-[(3-Fluoro-4-hydroxy-benzyl)-[1,2,4]triazol-4-yl-amino]-benzonitrile

https://huagongshe.com/reaction/19934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21976895HCID 21976895—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-[(3-Fluoro-4-hydroxy-benzyl)-[1,2,4]triazol-4-yl-amino]-benzonitrileHCID 21976903—

Reaction Steps

4-[(4-Benzyloxy-3-fluoro-benzyl)-[1,2,4]triazol-4-yl-amino]-benzonitrile (CAB03019, 2.83 g, 7.09 mmol) was dissolved in a mixture of ethanol (50 mL), THF (50 mL) and ethyl acetate (50 mL) by heating and palladium on charcoal (150 mg, 5% Pd) was added. The mixture was stirred under hydrogen-atmosphere (balloon) for 18 h, filtered through a 3 cm layer of celite and concentrated under reduced pressure. The residue was suspended in 2-propanol (30 mL), the mixture was heated to reflux for 5 minutes. After cooling room temperature the white precipitate was filtered off and dried under high vacuum. Yield: 2.13 g (97%). 1H-NMR (400, d6-DMSO)=4.93 (s, 2H), 6.75 (d, J=9.0 Hz, 2H), 6.82-6.89 (m, 2H), 7.07-7.12 (m, 1H), 7.76 (d, J=9.0 Hz, 2H), 8.77 (s, 2H), 9.95 (s, 1H, —OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745472B2
Source datasetuspto-grants-2010_06
ORD IDord-8d878a19d57748398994e4fe3a550ac0
Source noteuspto-grants-2010_06