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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056843Generated: October 31, 2026

4-Nitroindazole → NoName_3327

https://huagongshe.com/reaction/2056843

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 numberUS07335678B2
Source datasetuspto-grants-2008_02
ORD IDord-d1fb8f34d01b4f37bf8dcdcae76162e0
Source noteuspto-grants-2008_02