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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958674Generated: November 1, 2026

Hydrazine hydrate (1:1) → HCID 59160549, compound

https://huagongshe.com/reaction/1958674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 59160541HCID 59160541—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 59160549HCID 5916054982%

Reaction Steps

To a stirred solution of 6-(2-(4-fluoro-3-nitrobenzyl)-5-(6-methylpyridin-2-yl)-1H-imidazol-4-yl)quinoxaline (49.6 mg, 0.113 mmol, prepared according to the method described in US 2008/0319012 A1) in MeOH (5 mL) were added Raney Ni (0.1 mg, 10% w/w) and hydrazine monohydrate (0.027 mL, 0.563 mmol) and the mixture was stirred at room temperature for overnight. The reaction mixture was filtered through celite and the filtrate was concentrated under reduced pressure. The residue was purified by MPLC (MeOH:CH2Cl2=1:50 (v/v)) and on NH silica gel (MeOH:CH2Cl2=1:100 (v/v)) to afford the title compound (37.8 mg, 82%). (300 MHz, CDCl3) δ 1.99 (4H, m), 2.54 (3H, s), 3.23 (4H, t), 4.31 (2H, s), 6.37 (1H, dd), 6364 (1H, d), 6.95 (1H, d), 7.23-7.43 (5H, m), 7.98 (1H, dd), 8.08-8.17 (3H, m), 8.91 (1H, dd), 10.40 (1H, bs) MS (ESI) m/z 446 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410146B2
Source datasetuspto-grants-2013_04
ORD IDord-f25f549b26a14bb0a2c412c1a1ab8b60
Source noteuspto-grants-2013_04