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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823914Generated: October 30, 2026

5-Nitroindazole → HCID 178526490, compound

https://huagongshe.com/reaction/1823914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitroindazoleHCID 21501—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
ProductHCID 178526490HCID 17852649077.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Nitroindazole (10 g, 61.3 mmol) was dissolved in acetic acid (170 mL) and the mixture heated to 80° C. Bromine (3.1 mL, 60.7 mmol) was added slowly and the mixture heated to reflux. After 2 hours, the reaction mixture was allowed to cool to room temperature, and the resulting precipitate filtered off. Additional product was isolated by concentrating the filtrate, partitioning the residue between chloroform and saturated sodium bicarbonate solution, separating and drying the organic phase over sodium sulfate. Concentration gave a solid which was combined with the original precipitate to give the title compound as a yellow solid (11.4 g, 77%). 1H NMR δ 7.74 (1H, d), 8.21 (1H, dd), 8.40 (1H, d), 14.06 (1H, brs); MS (ES−) m/e=240.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041687B2
Source datasetuspto-grants-2006_05
ORD IDord-11e6ac8c8ddd4a7d9d418a9a9a11ce87
Source noteuspto-grants-2006_05