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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047523Generated: October 31, 2026

O-Phenylenediamine → 3-(1H-Benzo[d]imidazol-2-yl)-5-bromo-1H-indazole

https://huagongshe.com/reaction/1047523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 178520023HCID 178520023—
CatalystHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-(1H-Benzo[d]imidazol-2-yl)-5-bromo-1H-indazoleHCID 13582014550%

Reaction Steps

5-Bromo-1H-indazole-3-carbaldehyde (50 mg, 0.222 mmol) and o-phenylene diamine (24 mg, 0.222 mmol) were dissolved in dry THF (10 mL). One drop of 2N HCl was added. The solution was heated at a gentle reflux for 30 min and then 1N sodium bisulfite (1 mL) was added. After overnight at reflux, the solution was cooled to room temperature, and then diluted with ethyl acetate (30 mL). The mixture was washed with water and brine, dried over Na2SO4, and concentrated. Purification by flash chromatography (20% ethyl acetate/hexane) afforded the title compound as a pale yellow solid in a 50% yield. 1H NMR (400 MHz, CDCl3): δ 8.73 (d, 1H, J=1.2 Hz), 7.80 (m, 1H), 7.48-7.45 (m, 2H), 7.37 (d, 1H, J=8.8 Hz), 7.23 (m, 2H); ESI-MS [M+H]+: 313.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569511B2
Source datasetuspto-grants-2013_10
ORD IDord-0a5b981be7474585bf1659ce08bf6ab9
Source noteuspto-grants-2013_10