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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038708Generated: October 29, 2026

Triethylamine → 6-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbonitrile

https://huagongshe.com/reaction/2038708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant6-Bromo-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carbaldehydeHCID 86676267—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product6-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbonitrileHCID 7123777399%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 6-bromo-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carbaldehyde (Preparation 1, 60 g, 194 mmol) in MeCN (1.5 L) was added triethylamine (68.5 mL, 485 mmol) and hydroxylamine hydrochloride (20 g, 291 mmol). The reaction was heated at 60° C. for 3 hours. The reaction was cooled to 0° C., further triethylamine (220 mL, 1.55 mol) was added and TFAA (109 mL, 776 mmol) was added dropwise. The reaction was allowed to warm to room temperature and stirred for 2 hours. Water (2 L) was added to the reaction mixture and the resulting solid was collected by filtration. The solid was dissolved in DCM (1 L) and the resulting solution was washed with water (2×500 mL). The organic layer was dried over MgSO4 and concentrated in vacuo to give the title compound as a white solid (58.59 g) in a 99% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575336B2
Source datasetuspto-grants-2013_11
ORD IDord-cf5144fdd4614e029142117666097ed2
Source noteuspto-grants-2013_11