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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014279Generated: November 1, 2026

Hydrazine hydrate (1:1) → HCID 59441998, compound

https://huagongshe.com/reaction/1014279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 59442105HCID 59442105—
CatalystIron chloride (FeCl3)HCID 24380—
SolventMethanolHCID 887—
ProductHCID 59441998HCID 5944199819%

Reaction Conditions

Temperature64 °C

Reaction Steps

To N,N-dimethyl-3[5-(methyloxy)-6-nitro-2,3-dihydro-1H-indol-1-yl]-3-oxo-1-propanamine (1.52 g, 5.4 mmol) in MeOH (50 mL) was added iron (III) chloride (0.220 g, 1.35 mmol, Aldrich) and activated carbon (2.0 g, Aldrich). The reaction mixture was stirred at 64° C. for 20 min before the dropwise addition of hydrazine hydrate (1.2 mL, 37.5 mmol, Aldrich) over 5 min. The reaction was kept stirring at 64° C. for additional 12 h. Filtration removed the solids and the filtrate was concentrated and purified via chromatography on SiO2 (0-10% 2 M NH3 in MeOH/DCM) to afford 1-[3-(dimethylamino)propanoyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine (0.270 g, 19% Yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.72 (s, 1 H), 6.63 (s, 1 H), 3.95-4.15 (m, 2 H), 3.81 (s, 3 H), 3.76 (s, 2 H), 3.10 (t, J=8.43 Hz, 2 H), 2.83-2.96 (m, 2 H), 2.70 (t, J=7.15 Hz, 2 H), 2.41 (s, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-c231e2ca5d7343299bba0e1af7f3f8be
Source noteuspto-grants-2011_07