Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585956Generated: October 31, 2026

4-Nitroindazole → NoName_3327

https://huagongshe.com/reaction/585956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitroindazoleHCID 18057—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductNoName_3327HCID 41308575.1%

Reaction Steps

4-Nitro-1H-indazole (1.63 g, 10 mmol) in ethanol (100 mL) was treated with BiCl3 (3.46 g, 11 mmol) followed by a portionwise addition of NaBH4. The reaction mixture was stirred at ambient temperature for 20 minutes and filtered through Celite. The filtrate was evaporated under reduced pressure and the residue was partitioned between ethyl acetate/dilute NaHCO3 solution. The organic layer was dried over MgSO4, filtered, and the filtrate concentrated under reduced pressure to provide the title compound as a tan solid (1.0 g). 1H NMR (300 MHz, DMSO-d6) δ 5.64 (s, 2H), 6.1 (d, 1H), 6.6 (d, 1H), 6.98 (t, 1H), 8.03 (s, 1H), 12.6 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933311B2
Source datasetuspto-grants-2005_08
ORD IDord-8d6358c194e54995bceef18ee073e1e3
Source noteuspto-grants-2005_08