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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752550Generated: October 28, 2026

1H-Indazole → HCID 25165085, compound

https://huagongshe.com/reaction/1752550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-IndazoleHCID 9221—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
ReactantL-ProlineHCID 145742—
ReactantBenzylacetyleneHCID 575753—
ReactantSodium AscorbateHCID 23667548—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 25165085HCID 25165085—

Reaction Conditions

Temperature65 °C

Reaction Steps

Example 87A (969 mg, 3.39 mmol), 3-phenyl-1-propyne (392 mg, 3.37 mmol), sodium azide (278 mg, 4.28 mmol), sodium ascorbate (68 mg, 3.43 mmol), sodium carbonate (75 mg, 0.708 mmol), and L-proline (78 mg, 8.98 mmol) were combined in a 1:1 mixture of dimethyl sulfoxide and water (10 mL). Copper(II) sulfate pentahydrate (46 mg, 0.184 mmol) was added and the mixture was stirred at 65° C. for 3 hours. 6 N Sodium hydroxide (1 mL) was added, and the mixture was stirred for 30 minutes to deprotect the indazole. The mixture was diluted with ethyl acetate and washed with 1 N hydrochloric acid. The organic layer was concentrated under reduced pressure, and the resulting residue was triturated with methanol. The remaining solids were absorbed on silica gel and purified by silica gel chromatography eluting with a gradient of 0-5% methanol in dichloromethane to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 13.35 (s, 1H) 8.58 (s, 1H) 8.17-8.27 (m, 1H) 7.86 (d, J=8.82, 2.03 Hz, 1H) 7.67-7.77 (m, 1H) 7.27-7.36 (m, 2H) 7.18-7.27 (m, 1H) 4.10 (s, 1H). MS (ESI+) m/z 276.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163007B2
Source datasetuspto-grants-2015_10
ORD IDord-b9fc1d204f32463eb13aaf1ecfed526f
Source noteuspto-grants-2015_10