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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457336Generated: October 26, 2026

Water → 1-(4-acetylphenyl)-8-{[(2-chloropyridin-3-yl)carbonyl]amino}-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide

https://huagongshe.com/reaction/457336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantSodium BicarbonateHCID 516892—
Reactant8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-ethynylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamideHCID 22291546—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-acetylphenyl)-8-{[(2-chloropyridin-3-yl)carbonyl]amino}-4,5-dihydro-1H-benzo[g]indazole-3-carboxamideHCID 22291578—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-ethynylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide (442 mg, 1.2 mmol), water (65 mg, 3.6 mmol), and triflic acid (270 mg, 1.8 mmol) in dioxane (10 mL) was heated to 100° C. for 18 h. The mixture was cooled to RT, aqueous NaHCO3 was added, and filtered. The product was washed with water and ether, and dried. This gave product (293 mg, 67%). 1H NMR was consistent with its structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186743B2
Source datasetuspto-grants-2007_03
ORD IDord-5b2adc3a27b945769eb500b2a81b6e8b
Source noteuspto-grants-2007_03