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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186299Generated: October 31, 2026

Hydrazine hydrate (1:1) → HCID 57701048, compound

https://huagongshe.com/reaction/1186299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 57701037HCID 57701037—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 57701048HCID 5770104897.1%

Reaction Steps

To a solution of tert-butyl ethyl(3-(5-nitro-1H-indol-3-yl)cyclopentyl)carbamate (1.40, g 3.75 mmol) in dry MeOH (15 mL) was added Raney-Ni (0.1 g as a slurry in water) and hydrazine hydrate (1.9 mL, 37.5 mmol). The resulting mixture was immersed in a preheated oil bath and refluxed for 15 min. until the solution became clear. The reaction was cooled and filtered trough celite, washed with MeOH (20 mL) and the solvent evaporated. The crude was purified on column chromatography (2% 2N NH3 in MeOH: 98% CH2Cl2) to give the title compound as a brownish solid (1.25 g, quantitative). 1H-NMR (CDCl3) δ 1.11-1.19 (m, 6H), 1.49 (s, 18H), 1.67-1.89 (m, 6H), 1.96-2.12 (m, 4H), 2.13-2.22 (m, 2H), 2.26-2.35 (m, 2H), 3.10-3.28 (m, 4H), 3.37-3.58 (m, 4H), 4.44-4.59 (m, 2H), 6.64 (dd, 1H, J=1.8, 9.0 Hz), 6.67 (dd, 1H, J=2.1, 8.4 Hz), 6.91 (d, 1H, J=2.4 Hz), 6.92 (d, 1H, J=2.1 Hz), 7.14 (d, 1H, J=2.1 Hz), 7.17 (d, 1H, J=2.1 Hz), 7.73 (brs, 2H, NH); E1-MS (m/z, %) 343 (M+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673909B2
Source datasetuspto-grants-2014_03
ORD IDord-424cad5b6f6f4c3ea61736f6d5a85ee0
Source noteuspto-grants-2014_03